2011 Group Project 5: Difference between revisions
From Embryology
No edit summary |
No edit summary |
||
Line 15: | Line 15: | ||
= History of the disease = | = History of the disease = | ||
<ref><pubmed>6348096</pubmed></ref> | |||
Fragile X Syndrome is given its name due to an abnormality of the X chromosome. The abnormality arises from a site of constriction on the long arm of the chromosome X which is prone to breaking, resulting in a chromosomal lesion.<ref><pubmed>6348096</pubmed></ref> | |||
= Epidemiology = | = Epidemiology = |
Revision as of 11:10, 31 August 2011
Note - This page is an undergraduate science embryology student group project 2011. |
Your Project Goes Here. Oh yes it does!
Introduction to Fragile X Syndrome
Fragile X Syndrome does not create X-Men. Sad face.
History of the disease
Fragile X Syndrome is given its name due to an abnormality of the X chromosome. The abnormality arises from a site of constriction on the long arm of the chromosome X which is prone to breaking, resulting in a chromosomal lesion.[1]
Epidemiology
Etiology
Genetic Contribution
Development of the Disease
Fetal Development
At Birth
In Adult
Signs and Symptoms
Physical phenotype
Social interaction
Intellectual development
Recent Research
Autism and Fragile X Syndrome
Diagnosis
Treatment
References
- ↑ <pubmed>6348096</pubmed>
Glossary
2011 Projects: Turner Syndrome | DiGeorge Syndrome | Klinefelter's Syndrome | Huntington's Disease | Fragile X Syndrome | Tetralogy of Fallot | Angelman Syndrome | Friedreich's Ataxia | Williams-Beuren Syndrome | Duchenne Muscular Dystrolphy | Cleft Palate and Lip