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| valign="top"|The abnormal facial features are, as all other symptoms, based on the genetic changes of the chromosome 22. While there are broad variations amongst patients, common facial features can be seen in the image on the right <ref><pubmed>20573211</pubmed></ref>. | | valign="top"|The abnormal facial features are, as all other symptoms, based on the genetic changes of the chromosome 22. While there are broad variations amongst patients, common facial features can be seen in the image on the right <ref><pubmed>20573211</pubmed></ref>. | ||
| [[Image:DiGeorge_1.jpg|abnormal facial features observed in DiGeorge syndrome| | | [[Image:DiGeorge_1.jpg|abnormal facial features observed in DiGeorge syndrome| 150px]] | ||
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Revision as of 20:41, 12 September 2011
Note - This page is an undergraduate science embryology student group project 2011. |
DiGeorge Syndrome
--Mark Hill 10:54, 8 September 2011 (EST) There seems to be some good progress on the project.
- It would have been better to blank (black) the identifying information on this ultrasound.
- Historical Background would look better with the dates in bold first and the picture not disrupting flow (put to right).
- None of your figures have any accompanying information or legends.
- The 2 tables contain a lot of information and are a little difficult to understand. Perhaps you should rethink how to structure this information.
- Currently very text heavy with little to break up the content.
- I see no student drawn figure.
- referencing needs fixing, but this is minor compared to other issues.
Introduction
A congenital disorder is one which is present at birth. They are often abnormalities that arise from errors that occur during development of the fetus. Some congenital abnormalities are genetic, and often run in families while others are spontaneous and have no genetic linkages. DiGeorge syndrome is a congenital abnormality that is caused by the deletion of a part of chromosome 22. The symptoms and severity of the condition is thought to be dependent upon what part of and how much of the chromosome is absent. [1].
About 1/4000 children born are affected by DiGeorge syndrome, with 90% of these cases involving a deletion of a section of chromosome 22 [2]. DiGeorge is quite often a spontaneous mutation, but it may be passed on in an autosomal dominant fashion. Some families have many members affected.
DiGeorge is a complex syndrome and patient cases vary greatly. The common symptoms present across numerous patients include
- Congenital heart defects
- Defects of the palate/velopharyngeal insufficiency
- Recurrent infections due to immunodeficiency
- Hypocalcaemia due to hypoparathyrodism
- Learning difficulties
- Abnormal facial featuresds [3]
DiGeorge is a serious syndrome affecting many of the body systems. The clinical manifestations of the chromosome 22 deletion are significant and can lead to poor quality and a shortened lifespan for the patient. As there is currently no treatment education is vital to the wellbeing of those affected, directly or indirectly by this condition. [4] Current and future research is aimed at how to prevent and treat the condition, there is still a long way to go but some progress is being made.
Historical Background
- Angelo DiGeorge. In the mid 1960's, Angelo DiGeorge noticed a similar combination of clinical features in some children. He named the syndrom after himself. The symptoms that he recognised were hypoparathyroidism, underdeveloped thymus, conotruncal heart defects and a cleft lip/palate. [5]
- Robert Shprintzen described patients with similar symptoms (cleft lip, heart defects, absent or underdeveloped thymus, hypocalcemia) and named the group of symptoms as velo-cardio-facial syndrome. [6]
- Lischner and Huff determined that there was a deficiency in T cells was present in 10-20% of the normal thymic tissue of DiGeorge syndrome patients (1975). [7]
- Cleveland determined that a thymus transplant in patients of DiGeorge was able to restore immunlogical function (1975). [8]
- Finley and others identified that the cardiac failure of infants suffering from DiGeorge could be related to abnormal development of structures derived from the pouches of the 3rd and 4th pouches in the pharangeal arches. [9]
- 1980s technology develops to identify that these patients have part of a chromosome missing. [10]
- De La Chapelle suspects that a chromosome deletion in 22q11l is responsible for diGeorge syndrome (1981) [11]
- Ammann suspects that DiGeorge symdrome may be caused by alcoholism in the mother during pregnancy. There appears to be abnormalities between the two conditions such as facial features, cardiovascular, immune and neural symptoms (1982). [12]
- Muller observes the clinical features and natural history of DiGeorge (1989) [13]
- Pueblitz notes a deficiency in thyroid C cells in Digeorge patients (1993) [14]
- Crifasi uses FISH as a definitive diagnosis of DiGeorge (1995) [15]
- Davidson diagnoses DiGeorge prenatally using echocardiography and amniocentesis. This was the first reported case of prenatal diagnosis with no family history. (1998) [16]
- Matsumoto confirms bone marrow transplant as an effective therapy of DiGeorge syndrome (1998) [17]
- Lee links heart defects to the chromosome deletion in DiGeorge syndrome (2001) [18]
- Lu determines that the genetic factors leading to DiGeorge syndrome are linked to the clinical features of Tetralogy of Fallot. (2001) [19]
- Garg evaluates the role of TBx1 and Shh genes in the development of DiGeorge Syndrome (2001) [20]
- Rice expresses that while thymic transplantation is effective in restoring some immune function in Digeorge patients, the multifaceted disease requires a more rounded approach to treatment (2004) [21]
- Fagman identifies Tbx1 as the transcription factor that may be responsible for incorrect positioning of the thymus and other abnormalities in Digeorge (2007) [22]
- Oberoi uses speech, dental and velopharyngeal features as a method of diagnosing DiGeorge syndrome (2011) [23]
- Yang notices dental anomalies associated with 22q11 gene deletions (2005) [24]
Epidemiology
It appears that DiGeorge syndrome has a minimum incidence of about 1 per 2000-4000 live births in the general population, ranking the most frequent cause of genetic abnormality at birth, behind Down Syndrome [25]. Due to the fact that 22q11.2 deletions can also resulting in signs that are predictive of velocardiofacial syndrome as well, there is some confusion over the figures for epidemiology [26]. Due to these afore mentioned factors, it is therefore difficult to generate an exact figure for the epidemiology of DiGeorge syndrome; the 1 in 4000 live births is the minimum estimate of incidence [27]. For example, the study by Goodship et al examined 170 infants, 4 of which had a ventricular septal defect. This study, performed by directly examining the infants themselves produced an estimate of 1 in 3900 births, which is quite similar to the predicted value of 1 in 4000[28]. Other epidemiological analyses of DiGeorge syndrome, such as the study performed by Devriendt et al, have referred to birth defect registries, which produces an average value of 1 in 6935. However, this incidence is specific to Belgium, and does not represent the true incidence of DiGeorge syndrome [29].
The presentation of more severe cases of DiGeorge syndrome is apparent at birth, especially with malformations. The initial presentation of DiGeorge syndrome include hypocalcaemia, decreased T cell numbers, dysmorphic features, renal abnormalities and possibly a cardiac defect[30]. Cardiac defects present in about 75% of patients[31]. When the infant makes his/her first noises, if nasal in tone, then DiGeorge will be suspected. Other indications of DiGeorge syndrome are unusually high susceptibility to infection during the first six months of life, or abnormalities in facial features.
It has been well documented that there individuals who have relatively minor cardiac malformations and normal immune function, and may show no presentation of DiGeorge syndrome until later in life, which may be resultant form a learning dysfunction or heart disease. DiGeorge syndrome frequently presents with cleft palate, as well as congenital heart defects[32]. As would be suspected, it appears that cardiac complications are the largest causes of mortality. Infants face constant recurrent infection as a secondary result of T-cell immunodeficiency, caused by the hypoplastic thymus.
There is no preference to either sex or race [33]. Depending on the severity of DiGeorge syndrome, it can be diagnosed at varying ages. Those that present with cardiac symptoms can be diagnosed at birth; others may present much later in life and be diagnosed with DiGeorge (up to 50 years of age).
Etiology
DiGeorge Syndrome (DGS) is a developmental field defect that is caused by a 1.5- to 3.0-megabase hemizygous deletion in chromosome 22q11 [34]. This region is particularly susceptible to rearrangements that cause congenital anomaly disorders, namely; Cat-eye syndrome (tetrasomy), Der syndrome (trisomy) and VCFS (Velo-cardio-facial Syndrome)/DGS (Monosomy).
VCFS/DGS are the most common syndromes associated with 22q11 rearrangements, and as mentioned previously it has a prevalence of 1/2000 to 1/4000 [35].
The micro deletion locus is comprised of approximately 30 genes [36], with the TBX1 gene shown by mouse studies to be a major candidate DGS, as it is required for the correct development of the pharyngeal arches and pouches [37]. Comprehensive functional studies on animal models revealed that TBX1 is the only gene with haploinsufficiency that results in the occurrence of a phenotype characteristic for the 22q11.2 deletion Syndrome [38]].
Some reported cases show autosomal dominant, autosomal recessive, X-linked and chromosomal modes of inheritance for DGS. [39]. However more current research suggests that the majority of microdeletions are autosomal dominant, with 93% of these cases originating from a de novo deletion of 22q11.2 and with 7% inheriting the deletion from a parent [40].
Cytogenetic studies indicate that about 15-20% of patients with DGS have chromosomal abnormalities, and that almost all of these cases are either unbalanced translocations with monosomy or interstital deletions of chromosome 22. [41]
A recent study supported this by showing a 14.98% presence of microdeletions in 22q11.2 for a group of 87 children with DGS symptoms. This same study, by Wosniak Et Al 2010, showed that 90% of patients the microdeletion covered the region of 3 Mbp, encoding the full 30 genes [42].
Whereas a microdeletion of 1.5 Mbp including 24 genes was been found in 8% of patients. A minimal DiGeorge critical region (MDGCR) is said to cover about 0.5 Mbp and several genes[43]. The remaining 2% included patients with other chromosomal aberrations. [44]
*Still more to come on this guys, as well as a bit of restructuring.. working on the research possibilities subheading aswell. Again, sorry to hold you up. -- Timothy Ellwood 21:13, 5 September 2011 (EST)
Pathogenesis/Pathophysiology
As mentioned in the introduction, the pathogenesis of DiGeorge is a 22q11.2 microdeletion.
DiGeorge is a result of a 2-3million base pair deletion from the long arm of chromosome 22. It seems that this particular region in chromosome 22 is particularly vulnerable to microdeletions, which usually occur during meiosis. These microdeletions also tend to be new microdeletions, hence DiGeorge can present in families that have no history of DiGeorge syndrome. However, DiGeorge can also be inherited in an autosomal dominant manner [45].
There are multiple genes responsible for similar function in the region, resulting in similar symptoms being seen across a large number of 22q11.2 microdeletion syndromes. This means that all 22q11.2 microdeletion syndromes have very similar presentation, making the exact pathogenesis difficult to treat, and unfortunately DiGeorge syndrome is well known by several other names, including (but not limited to) Velocardiofacial syndrome (VCFS), Conotruncal anomalies facie (CTAF) syndrome, as well as CATCH-22 syndrome[46]. The acronym of CATCH-22 also describes many signs of which DiGeorge syndrome presents with, including Cardiac defects, Abnormal facial features, Thymic hypoplasia, Cleft palate, and Hypocalcemia. Variants also include Burn’s proposition of Cardiac abnormality, T cell deficit, Clefting and Hypocalcemia.
Genes involved in DiGeorge syndrome
The specific gene that is critical in development DiGeorge syndrome when deleted is the ‘‘TBX1’’ gene[47]. The ‘‘TBX1’’ chromosomal section results in the failure of the third and fourth pharyngeal pouches to develop, resulting in several signs and symptoms which are present at birth. These include thymic hypoplasia, hypoparathyroidism, recurrent susceptibility to infection, as well as congenital cardiac abnormalities, craniofacial dysmorphology and learning dysfunctions[48]. These symptoms are also accompanied from hypocalcemia as a direct result of the hypoparathyroidism; however, this may resolve within the first year of life. ‘‘TBX1’’ is expressed in early development in the pharyngeal arches, pouches and otic vesicle; and in late development, in the vertebral column and tooth bud. This loss of ‘‘TBX1’’ results in the cardiac malformations that are observed. It is also important in the regulation of paired-like homodomain transcription factor 2 (PITX2), which is important for body closure, craniofacial development and asymmetry for heart development. This gene is also expressed in neural crest cells, which leads to the behavioral and cognitive disturbances commonly seen[49]. The ‘‘Crkl’’ gene is also involved in the development of animal models for DiGeorge syndrome.
Structures formed by the 3rd and 4th pharyngeal pouches
Embryologically, the 3rd and 4th pharyngeal pouches are structures that are formed in between the pharyngeal arches during development. [50]
The thymus is primarily active during the perinatal period and is developed by the third pharyngeal pouch, where it provides an area for the development of regulatory T cells. The parathyroid glands are developed from both the third and fourth pouch.
Pathophysiology of DiGeorge syndrome
There are two main physiological points to discuss when considering the presentation that DiGeorge syndrome has. Apart from the morphological abnormalities, we can discuss the physiology of DiGeorge below.
Hypocalcemia
Hypocalcemia is a result of the parathyroid hypoplasia. Parathyroid hormone (PTH) is the main mechanism for controlling extracellular calcium and phosphate concentrations, and acts on the intestinal absorption, renal excretion and exchange of calcium between bodily fluids and bones. The lack of growth of the parathyroid glands results in a lack of PTH resulting in the observed hypocalcemia[51].
Decreased Immune Function
Hypoplasia of the thymus is also observed in the early stages of DiGeorge syndrome. The thymus is the organ located in the anterior mediastinum and is responsible for the development of T-lymphocytes in the embryo. It is crucial in the early development of the immune system as it is involved in the exposure of lymphocytes into thousands of different antigens, providing an early mechanism of immunity for the developing child. The second role of the thymus is to ensure that these lymphocytes that have been sensitized do not react to any antigens presented by the body’s own tissue, and ensures that they only recognize foreign substances. The thymus is primarily active before parturition and the first few months of life[52]. Hence, we can see that if there is hypoplasia of the thymus gland in the developing embryo, the child will be more likely to get sick due to a weak immune system.
Dianostic Tests
Fluorescence in situ hybridisation (FISH)
Technique | Image |
FISH is a technique that attaches DNA probes that have been labeled with fluorescent dye to chromosomal DNA. [53] When viewed under fluorescent light, the labelled regions will be visible. This test allows for the determination of whether or not chromosomes or parts of chromosomes are present. This procedure differs from others in that the test does not have to take place during cell division. [54] FISH is a significant test used to confirm a DiGeorge diagnosis. Since the syndrome features a loss of part or all of chromosome 22, the probe will have nothing or little to attach to. This will present as limited fluorescence under the light and the diagnostician will determine whether or not the patient has DiGeorge. As with any testing, it is difficult to rely on one result to determine the condition. The patient must present with certain clinical features and then FISH is used to confirm the diagnosis. | ![]() |
Based on symptoms
Technique | Image |
DiGeorge patients often have similar symptoms even though it is a condition that affects a number of the body systems. These similarities can be used as early tools in diagnosis. Practitioners would be looking for features such as the following:
|
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Ultrasound
Technique | Image |
An ultrasound is a prenatal care test to determine how the fetus is developing and whether or not any abnormalities may be present. The machine sends high frequency sound waves into the area being viewed. The sound waves reflect off of internal organs and the fetus into a hand held device that converts the information onto a monitor to visualize the sound information. Ultrasound is a non-invasive procedure. [56]
Ultrasound is able to pick up any abnormalities with heart beats. If the heart has any abnormalities is will lead to further investigations to determine the nature of these. It can also be used to note any physical abnormalities such as a cleft palate or an abnormally small head. Like diagnosis based on clinical features, ultrasound is used as an early indication that something may be wrong with the fetus. It leads to further investigations. |
Amniocentesis
Technique | Image |
Amniocentesis is a medical procedure where the practitioner takes a sample of amniotic fluid in the early second trimester. The fluid is obtained by pressing a needle and syringe through the abdomen. Fetal cells are present in the amniotic fluid and as such genetic testing can be carried out.
Amniocentesis is performed around week 14 of the pregnancy. As DiGeorge symdrome presents with missing or incomplete chromosome 22, genetic testing is able to determine whether or not the child is affected. 95% of DiGeorge cases are diagnosed using amniocentesis. [57] |
BACS- on beads technology
Technique | Image |
BACS on beads technology is a fast, cost effective alternative to FISH. 'BACS' stands for Bacterial Artificial Chromosomes. The DNA is treated with fluorescent markers and combined with the BACs beads. The beads are passed through a cytometer and they are analysed. The amount of fluorescence detected is used to determine whether or not there is an abnormality in the chromosomes.This technology is relatively new and at the moment is only used as a screening test. FISH is used to validate a result.
BACs is effective in picking up microdeletions. DiGeorge has microdeletions on the 22nd chromosome and as such is a good example of a syndrome that could be diagnosed with BACs technology. [58] |
http://www.ngrl.org.uk/Wessex/downloads/tm10/TM10-S2-3%20Susan%20Gross.pdf |
Clinical Manifestations
A syndrome is a condition characterized by a group of symptoms, which either consistently occur together or vary amongst patients. While all DiGeorge cases are caused by deletion of genes on the same chromosome, clinical phenotypes and abnormalities are variable [59]. The deletion has potential to affect almost every body system. However, the body systems involved, the combination and the degree of severity vary widely, even amongst family members [60] [61]. The most common signs and symptoms include:
- Congenital heart defects
- Defects of the palate/velopharyngeal insufficiency
- Recurrent infections due to immunodeficiency
- Hypocalcaemia due to hypoparathyrodism
- Learning difficulties
- Abnormal facial features
A combination of the features listed above represents a typical clinical picture of DiGeorge Syndrome [62]. Therefore these common signs and symptoms often lead to the diagnosis of DiGeorge Syndrome and will be described in more detail in the following table. It should be noted however, that up to 180 different features are associated with 22q11.2 deletions, often leading to delay or controversial diagnosis [63].
Abnormality | Clinical presentation | How it is caused | |
Congenital heart defects | Congenital malformations of the heart can present with varying severity ranging from minimal symptoms to mortality. In more severs cases, the abnormalities are detected during pregnancy or at birth, where the infant presents with shortness of breath. More often however, no symptoms will be noted during childhood until changes in the pulmonary vasculature become apparent. Then, typical symptoms are shortness of breath, purple-blue skin, loss of consciousness, heart murmur, and underdeveloped limbs and muscles. These changes can usually be prevented with surgery if detected early [64] [65]. | Congenital heart defects are commonly due to faulty development from the 3rd to the 8th week of embryonic development. Cardiac development includes looping of the heart tube, segmentation and growth of the cardiac chambers, development of valves and the greater vessels. Some of the genes involved in cardiac development are located on chromosome 22 [66] and in case of deletion can lead to various congenital heard disease. Some of the most common ones include patient ductus arteriosus, tetralogy of Fallot, ventricular septal defects and aortic arch abnormalities [67]. To give one example, the tetralogy of Fallot will be described and illustrated in image on the right. | |
Defect of palate/velopharyngeal insufficiency | Velopharyngeal insufficiency or cleft palate is the failure of the roof of the mouth to close during embryonic development. Apart from facial abnormalities when the upper lip is affected as well, a cleft palate presents with hypernasality (nasal speech), nasal air emission and in some cases with feeding difficulties [68]. The from a cleft palate resulting speech difficulties will be discussed in the image on the right. | The roof of the mouth, also called soft palate or velum, the posterior pharyngeal wall and the lateral pharyngeal walls are the structures that come together to close off the nose from the mouth during speech. Incompetence of the soft palate to reach the posterior pharyngeal wall is often associated with cleft palate. A cleft palate occur due to failure of fusion of the two palatine bones (the bone that form the roof of the mouth) during embryologic development and commonly occurs in DiGeorge syndrome [69]. | |
Recurrent infections due to immunodeficiency | Many newborns with a 22q11.2 deletion present with difficulties in mounting an immune response against infections or with problems after vaccination. it should be noted, that the variability amongst patients is high and that in most cases these problems cease before the first year of life. However some patients may have a persistent immunodeficiency and develop autoimmune diseases such as juvenile rheumatoid arthritis or graves disease [70]. | The immune system has a specialized T-cell mediated immune response in which T-cells recognize and eliminate (kill) foreign antigens (bacteria, viruses etc.) [71]. T-cells arise from and mature in the thymus. Especially during childhood T-cells arise from haemapoietic stem cells and undergo a selection process. In embryonic development the thymus develops from the third pharyngeal pouch, a structure at which abnormalities occur in the event of a 22q11.2 deletion. Hence patients with DiGeorge syndrome have failure in T-cell mediated response due to hypoplasticity or lack of the thymus and therefore difficulties in dealing with infections [72].
Autoimmune diseases are thought to be due to T-cell regulatory defects and impair of tolerance for the body's own tissue [73]. | |
Hypocalcaemia due to hypoparathyrodism | Hypoparathyrodism (lack/little function of the parathyroid gland) causes hypocalcaemia (lack/low levels of calcium in the bloodstream). Hypocalcaemia in turn may cause seizures in the fetus [74]. However symptoms may as well be absent until adulthood. Typical signs and symptoms of hypoparathyrodism are for example seizures, muscle cramps, tingling in finger, toes and lips, and pain in face, legs, and feet[75]. | The superior parathyroid glands as well as the parafollicular cells are formed from arch four in embryologic development and the inferior parathyroid glands are formed from arch three. Developmental failure of these arches may lead to incompletion or absence of parathyroid glands in DiGeorge. The parathyroid gland normally produces parathyroid hormone, which functions by increasing calcium levels in the blood. However in the event of absence or insufficiency of the parathyroid glands calcium deposits in the bones to increased amounts and calcium levels in the blood are decreased, which can cause sever problems if left untreated [76]. | |
Learning difficulties | Nearly all individuals with 22q11.2 deletion syndrome have learning difficulties, which are commonly noticed in primary school age. These learning difficulties include difficulties in solving mathematical problems, word problems and understanding numerical quantities. The reading abilities of most patients however, is in the normal range [77].
DiGeorge syndrome children appear to have an IQ in the lower range of normal or mild mental retardation[78]. |
While the exact reason for these learning difficulties remains unclear, studies show correlation between those and functional as well as structural abnormalities within the frontal and parietal lobes (front and side parts of the brain) [79]. Additionally studies found correlation between 22q11.2 and abnormally small parietal lobes [80]. | |
Abnormal facial features | To the common facial features of individuals with DiGeorge Syndrome belong [81]:
|
The abnormal facial features are, as all other symptoms, based on the genetic changes of the chromosome 22. While there are broad variations amongst patients, common facial features can be seen in the image on the right [82]. | ![]() |
Treatment
There is no cure for DiGeorge syndrome. Once a gene has mutated in the embryo de novo or has been passed on from one of the parents, it is not reversible [83]. However many of the associated symptoms, such as congenital heart defects, velopharyngeal insufficiency or recurrent infections, can be treated. As mentioned in clinical manifestations, there is a high variability of symptoms, up to 180, and the severity of these [84]. This often complicates the diagnosis. In fact, some patients are not diagnosed until early adulthood or not diagnosed at all, especially in developing countries [85] [86]. Once diagnosed, there is no single therapy plan. Opposite, each patient needs to be considered individually and consult various specialists, from example a cardiologist for congenital heard defect, a plastic surgeon for a cleft palet or an immunologist for recurrent infections, in order to receive the best therapy available. Furthermore, some symptoms can be prevented or stopped from progression if detected early. Therefore, it is of importance to diagnose DiGeorge syndrome as early as possible [87]. Despite the high variability, a range of typical symptoms raise suspicion for DiGeorge over a range of ages and will be listed below [88][89]:
- Newborn: heart defects
- Newborn: cleft palate, cleft lip
- Newborn: seizures due to hypocalcaemia
- Newborn: other birth defects such as kidney abnormalities or feeding difficulties
- Late-occurring features: autoimmune disorders (for example, juvenile rheumatoid arthritis or Grave's disease)
- Hypocalcaemia
- Psychiatric illness (for example, DiGeorge syndrome patients have a 20-30 fold higher risk of developing schizophrenia)
Once alerted, one of the diagnostic tests discussed above can bring clarity.
The treatment plan for DiGeorge syndrome will be both treating current symptoms and preventing symptoms. A range of conditions and associated medical specialties should be considered. Some important and common conditions will be discussed in more detail in the table below.
Cardiology
Therapy options for congenital heart diseases |
The classical treatment for severe cardiac deficits is surgery, where the surgical prognosis depends on both other abnormalities caused DiGeorge syndrome, such as a deprived immune system and hypocalcaemia, and the anatomy of the cardiac defects [90]. In order to achieve the best outcome timing is of importance [91].
Overall techniques in cardiac surgery have been adapted to the special conditions of patients with 22q11.2 deletion, which decreased the mortality rate significantly [92]. |
Plastic Surgery
Therapy options for cleft palate |
Plastic surgery in clef palate patients is performed to counteract the symptoms. Here, two opposing factors are of importance: first, the surgery should be performed relatively late, so that growth interruption of the palate is kept to a minimum. Second, the surgery should be performed relatively early in order to facilitate good speech acquisition. Hence there is the option of surgery in the first few moth of life, or a removable orthodontic plate can be used as transient palatine replacement to delay the surgery[93]. Outcomes of surgery show that about 50 percent of patients attain normal speech resonance while the other 50 percent retain hypernasality [94]. However, depending on the severity, resonance and pronunciation problems can be reversed or reduced with speech therapy [95]. |
Immunology
Therapy options for immunodeficiency |
The immune problems in children with DiGeorge syndrome should be identified early, in order to take special precaution to prevent infections and to avoiding blood transfusions and life vaccines [96]. Part of the treatment plan would be to monitor T-cell numbers [97]. A thymus transplant to restore T-cell production might be an option depending on the condition of the patient. However it is used as last resort due to risk of rejection and other adverse effects [98]. |
Endocrinology
Therapy options for hypocalcaemia |
Hypocalcaemia is treated with calcium and vitamin D supplements. Calcium levels have to be monitored closely in order to prevent hypercalcaemic (too high blood calcium levels) or hypocalcaemic (too low blood calcium levels) emergencies and possible calcification of tissue in the kidney [99]. |
Current and Future Research
Glossary
Antigen a substance or molecule which will trigger an immune response when introduced into the body
Arch of aorta first part of the aorta (major blood vessel from heart)
Autoimmune of or relating to disease caused by antibodies or lymphocytes produced against substances naturally present in the body (against oneself)
Autoimmune disease caused by mounting of an immune response including antibodies and/or lymphocytes against substances naturally present in the body
Autosomal Dominant is a method by which diseases can be passed down through families. It refers to a disease that only requires one copy of the abnormal gene to acquire the disease
Chromosome genetic material in each nucleus of each cell arranged and condensed strands. In humans there are 23 pairs of chromosomes of which 22 pairs make up autosomes and one pair the sex chromosomes
Cleft Palate refers to the condition in which the palate at the roof of the mouth fails to fuse, resulting in direct communication between the nasal and oral cavities
Congenital preset from birth
Ductus arteriosus duct from the pulmonary trunk (the blood vessel that pumps blood from the heart into the lung) to the aorta that closes after birth
Dysmorphia refers to the abnormal formation of parts of the body.
Graves disease symptoms due to too high loads of thyroid hormone, caused by an overactive thyroid gland
Haemapoietic stem cells multipotent cells that give rise to all blood cells
Hypocalcaemia deficiency of calcium in the blood stream
Hypoparathyrodism diminished concentration of parthyroid hormone in blood, which causes deficiencies of calcium and phosphorus compounds in the blood and results in muscular spasm
Hypoplasia refers to the decreased growth of specific cells/tissues in the body
Immunodeficiency insufficiency of the immune system to protect the body adequately from infection
Lateral anatomical expression meaning of, at towards, or from the side or sides
Malformation see dysmorphia
Palate the roof of the mouth, separating the cavities of the nose and the mouth in vertebraes
Parathyroid glands four glands that are located on the back of the thyroid gland and secrete parathyroid hormone
Parathyroid hormone regulates calcium levels in the body
Pharynx part of the throat situated directly behind oral and nasal cavity, connecting those to the oesophagus and larynx
Phenotype set of observable characteristics of an individual resulting from a certain genotype and environmental influences
Platelets round and flat fragments found in blood, involved in blood clotting
Posterior anatomical expression for further back in position or near the hind end of the body
Renal of or relating to the kidneys
Rheumatoid arthritis a chronic disease causing inflammation in the joints resulting in painful deformity and immobility especially in the fingers, wrists, feet and ankles
Schizophrenia a long term mental disorder of a type involving a breakdown in the relation between thought, emotion and behaviour, leading to faulty perception, inappropriate actions and feelings, withdrawal from reality and personal relationships into fantasy and delusion, and a sense of mental fragmentation. There are various different types and degree of these.
Seizure fit, very high neurological activity in the brain that causes wild thrashing movements
Sign an indication of a disease detected by a medical practitioner even if not apparent to the patient
Symptom a physical or mental feature that is regarded as indicating a condition of a disease, particularly features that are noted by the patient
Syndrome group of symptoms that consistently occur together or a condition characterized by a set of associated symptoms
T-cell a lymphocyte that is produced and matured in the thymus and plays an important role in immune response
Tetralogy of Fallot is a congenital heart defect
Third Pharyngeal pouch pocked-like structure next to the third pharyngeal arch, which develops into neck structures
Thyroid Gland large ductless gland in the neck that secrets hormones regulation growth and development through the rate of metabolism
Ventricular septum membranous and muscular wall that separates the left and right ventricle
References
- ↑ http://www.ncbi.nlm.nih.gov/books/NBK22179/
- ↑ http://www.bbc.co.uk/health/physical_health/conditions/digeorge1.shtml
- ↑ http://emedicine.medscape.com/article/135711-overview
- ↑ http://www.bbc.co.uk/health/physical_health/conditions/digeorge1.shtml
- ↑ http://www.chw.org/display/PPF/DocID/23047/router.asp
- ↑ http://digital.library.pitt.edu/c/cleftpalate/pdf/e20986v15n1.11.pdf
- ↑ <pubmed>1096976</pubmed>
- ↑ <pubmed>1148386</pubmed>
- ↑ <pubmed>4854619</pubmed>
- ↑ http://www.chw.org/display/PPF/DocID/23047/router.asp
- ↑ <pubmed>7250965</pubmed>
- ↑ <pubmed>6812410</pubmed>
- ↑ <pubmed>3044796</pubmed>
- ↑ <pubmed> 8372031 </pubmed>
- ↑ <pubmed>7490915</pubmed>
- ↑ <pubmed> 9160392</pubmed>
- ↑ <pubmed>9827824</pubmed>
- ↑ <pubmed>1488286</pubmed>
- ↑ <pubmed>11455393</pubmed>
- ↑ <pubmed>11412027</pubmed>
- ↑ <pubmed>15547821</pubmed>
- ↑ <pubmed>17164259</pubmed>
- ↑ <pubmed>21721477</pubmed>
- ↑ <pubmed>16252847</pubmed>
- ↑ PMC1051442
- ↑ PMID 8230155
- ↑ http://www.sciencedirect.com/science/article/pii/S0140673607616018
- ↑ PMID 9875047
- ↑ 9733045
- ↑ PMID 9875047
- ↑ http://omim.org/entry/188400
- ↑ PMID 21846625
- ↑ PMID 20301696
- ↑ PMC2871720
- ↑ PMC11715041
- ↑ PMC21134246
- ↑ PMC11971873
- ↑ PMC11971873
- ↑ PMC3146281
- ↑ PMC20301696
- ↑ PMC1715550
- ↑ PMC21134246
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- ↑ 9733045
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- ↑ PMID 20301696
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- ↑ <pubmed> PMID 17950858 </pubmed>
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- ↑ Guyton A, Hall J, Textbook of Medical Physiology, 11th Edition, Elsevier Saunders publishing, Chapter 34, p. 440-441
- ↑ http://www.springerlink.com/content/u3t2g73352t248ur/fulltext.pdf
- ↑ http://www.genome.gov/10000206
- ↑ http://www.chw.org/display/PPF/DocID/23047/router.asp
- ↑ http://www.betterhealth.vic.gov.au/bhcv2/bhcarticles.nsf/pages/Ultrasound_scan
- ↑ http://medical-dictionary.thefreedictionary.com/DiGeorge+syndrome
- ↑ http://www.ngrl.org.uk/Wessex/downloads/tm10/TM10-S2-3%20Susan%20Gross.pdf
- ↑ PMID 21049214
- ↑ <pubmed>9475599</pubmed>
- ↑ <pubmed>14736631</pubmed>
- ↑ PMID 21049214
- ↑ <pubmed>16027702</pubmed>
- ↑ Kumar, V., Abbas, A., Fausto, N., Mitchell, R. N. (2007). Robbins Basic Pathology. In Saunders Elsevier (Ed 8), Philadelphia. https://evolve.elsevier.com/productPages/s_1221.html
- ↑ <pubmed>18636635</pubmed>
- ↑ Kumar, V., Abbas, A., Fausto, N., Mitchell, R. N. (2007). Robbins Basic Pathology. In Saunders Elsevier (Ed 8), Philadelphia. https://evolve.elsevier.com/productPages/s_1221.html
- ↑ <pubmed> 18770859 </pubmed>
- ↑ PMID: 21861138
- ↑ <pubmed>21738760</pubmed>
- ↑ PMID 21049214
- ↑ Kumar, V., Abbas, A., Fausto, N., Mitchell, R. N. (2007). Robbins Basic Pathology. In Saunders Elsevier (Ed 8), Philadelphia. https://evolve.elsevier.com/productPages/s_1221.html
- ↑ <pubmed>19521511</pubmed>
- ↑ <pubmed<21049214<pubmed/>
- ↑ <pubmed>21049214</pubmed>
- ↑ <pubmed></pubmed>18956803
- ↑ <pubmed>448529</pubmed>
- ↑ <pubmed>19213009</pubmed>
- ↑ <pubmed>17845235</pubmed>
- ↑ <pubmed>17928237</pubmed>
- ↑ <pubmed>11339378</pubmed>
- ↑ <pubmed>20573211</pubmed>
- ↑ <pubmed>20573211</pubmed>
- ↑ PMID 21049214
- ↑ <pubmed>16027702</pubmed>
- ↑ <pubmed>16027702</pubmed>
- ↑ <pubmed>15754359</pubmed>
- ↑ PMID 21274400
- ↑ <pubmed>16027702</pubmed>
- ↑ <pubmed>9350810</pubmed>
- ↑ <pubmed>18636635</pubmed>
- ↑ <pubmed>2811420</pubmed>
- ↑ <pubmed>5696314</pubmed>
- ↑ <pubmed>11772163</pubmed>
- ↑ <pubmed> 21740170</pubmed>
- ↑ <pubmed>8884403</pubmed>
- ↑ PMID 21049214
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- ↑ <pubmed>17284531</pubmed>
- ↑ <pubmed>20094706</pubmed>
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