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{{Header}}
==Introduction==
==Introduction==
[[File:Fetal_size_change.jpg|thumb|Fetal size change]]
[[File:Fetal_size_change.jpg|thumb|Fetal size change]]
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:{{Template:Fetal Links}}
{{Fetal Links}}


[[:Category:Second Trimester|Category:Second Trimester]]


==Some Recent Findings==
{|
|-bgcolor="F5FAFF"
|
* '''{{second trimester}} Serum Biomarker Screen for Fetal Aneuploidies as a Predictor of {{preterm birth}}: A Population-Based Study'''{{#pmid:30602167|PMID30602167}}  "To determine the association between second-trimester serum Down syndrome screening (alpha-fetoprotein [AFP] free beta-human chorionic gonadotropin [b-hCG] unconjugated estriol [uE3]) and preterm birth and to create predictive models for preterm birth. Secondary analysis on a prospective database of pregnancies undergoing second-trimester screen with complete follow-up. The multiples of medians (MoM) of the biomarkers were compared between the group of term, preterm (< 37 weeks), early preterm (< 34 weeks), and very early preterm (< 32 weeks) delivery. Predictive models were developed based on adjusted MoMs and logistic regression and diagnostic performances in predicting preterm birth were determined. ...The second trimester Down syndrome screening could also be used as a tool of risk identification of preterm birth in the same test, without extra-effort and extra-cost."


==Neural Development==
* '''{{Vitamin D}} - Lower vitamin D levels during the second trimester are associated with developing gestational diabetes mellitus: an observational cross-sectional study'''{{#pmid:30599810|PMID30599810}}
The images below are from a recent MRI study of fixed fetal brains at different weeks of development during the second trimester.<ref><pubmed>19339620</pubmed></ref>
In this study, we aimed to compare serum 25(OH)D levels in women with and without gestational diabetes mellitus (GDM), and to identify the serum 25(OH)D levels associated with GDM. We recruited 40 women with GDM and 40 healthy pregnant women, aged 20-40 years and in the second trimester, at Gulhane Education and Research Hospital. We excluded women with chronic diseases, preeclampsia, pre-GDM, multiple pregnancies, and those taking medications related to calcium or vitamin D metabolism. We took anthropometric measurements and blood samples during the second trimester. Of the 80 pregnant women, pre-pregnancy body mass index was significantly higher among the GDM group than the healthy group (26.4 ± 5.73 kg/m2 vs. 22.6 ± 3.56 kg/m2, p = .001). Serum 25(OH)D levels in women with GDM were significantly lower than those in healthy women (16.8 ± 9.90 ng/mL vs. 20.9 ± 8.16 ng/mL, p = .016). The prevalence of severe vitamin D deficiency was as high as 72.5% among women in the GDM group, with a 1.74-fold increased risk of deficient status. Levels of 25(OH)D lower than a cutoff value of 14.0 ng/mL were determined to be related to GDM. These study results suggest that maternal vitamin D deficiency in mid-pregnancy is significantly associated with development of GDM."
<gallery>
File:Brain fissure development 02.jpg|Three-dimensional reconstruction of the lateral (top row) and medial (bottom row) surface of 13–21 week brains to reveal the development of the Sylvian fissure or lateral sulcus (green arrow), the calcarine fissure (blue arrow), and the parieto-occipital sulcus (red arrow), respectively.
File:Brain tract development 06.jpg|3D depiction of developmental white matter fibers. A lateral view of limbic tracts where pink fibers in 13, 15, and 19 week brains are the fornix and stria terminalis and purple fibers in the 19 week brains indicate the cingulum bundle.
File:Brain ventricles and ganglia development 02.jpg|Three-dimensional reconstruction of the basal ganglia and ganglionic eminence. Different colors represent different brain structures: whole brain (gray), ventricle (pink), ganglionic eminence (red), putamen and globus pallidus together (cyan), thalamus (yellow), and caudate nucleus (green).
File:Brain fissure development 03.jpg|Three-dimensional reconstruction of the lateral (top row) and medial (bottom row) surface of 13–21 week brains to reveal the development of the Sylvian or lateral fissure (green arrow).
</gallery>
 
==Second Trimester Timeline==
 
(Clinical Week 14)
 
{| class="prettytable"
| <center>'''Week'''</center>
| <center>'''Stage'''</center>
| '''Event'''


|}
{| class="wikitable mw-collapsible mw-collapsed"
! More recent papers &nbsp;
|-
|-
| <center>12</center>
| [[File:Mark_Hill.jpg|90px|left]] {{Most_Recent_Refs}}
| Clinical second trimester
| [[File:Fetal_head_lateral.jpg|100px]]Week 12 - CRL 85 mm, femur length 15 mm, biparietal diameter 25 mm


[[Sensory_-_Hearing_and_Balance_Development|Hearing]] Week 12-16 - Capsule adjacent to membranous labrynth undegoes vacuolization to form a cavity (perilymphatic space) around membranous labrynth and fills with perilymph
Search term: [http://www.ncbi.nlm.nih.gov/pubmed/?term=Second+Trimester ''Second Trimester'']
 
[http://embryology.med.unsw.edu.au/Notes/genital.htm Genital]  male and female external genital differences observable
 
[[Respiratory_System_Development|Respire]] Month 3-6 - lungs appear glandular, end month 6 alveolar cells type 2 appear and begin to secrete surfactant
 
[[Tongue_Development|Tongue]] Week 12 - first differentiated epithelial cells (Type II and III)
 
female genital canal (80 days) formed with absorption of the median septum


|}
{| class="wikitable mw-collapsible mw-collapsed"
! Older papers &nbsp;
|-
|-
| <center>13</center>
| {{Older papers}}
| &nbsp;
* '''Review - Second trimester sonographic features of fetal chromosomal defects'''{{#pmid:24858178|PMID24858178}} "Advances in ultrasound technology have dramatically improved the detection of fetal chromosomal defects. Each chromosomal defect has its own syndromal pattern of detectable abnormalities prenataly. Most commonly detectable defects are Trisomies & Triploidies. Although only an invasive test can provide a definitive diagnosis, fetuses with major chromosomal abnormalities have either external or internal defects that can be recognized by detailed ultrasonographic examination at second trimester. These are defined as ultrasound markers for fetal aneuploidy. This article provides an overview and discussion on prenatal sonographic features that may suggest the presence of a common fetal chromosomal defect." {{Ultrasound}}
| [[Tongue_Development|Tongue]] Week 12 to 13 - maximum synapses between cells and afferent nerve fibers


&nbsp;
* Review - Second- and third-trimester biochemical and ultrasound markers predictive of ischemic placental disease.{{#pmid:24836829|PMID24836829}} "Ischemic placental disease is a recently coined term that describes the vascular insufficiency now believed to be an important etiologic factor in preeclampsia, intrauterine fetal growth restriction, and placental abruption. Given the increased risk for poor maternal and fetal outcomes, early prediction and prevention of this disorder is of significant clinical interest for many. In this article, we review the second- and third-trimester serum and ultrasound markers predictive of ischemic placental disease. Limited first-trimester data is also presented. While current studies report a statistical association between marker levels and various adverse perinatal outcomes, the observed diagnostic accuracy is below the threshold required for clinical utility. An exception to this generalization is uterine artery Doppler for the prediction of early-onset preeclampsia. Metabolomics is a relatively new analytic platform that holds promise as a first-trimester marker for the prediction of both early- and late-onset preeclampsia."
|}
==Neural Development==
[[File:Neural-development.jpg|thumb|400px|Timeline of events in Normal Human Neural Development<ref>Report of the Workshop on Acute Perinatal Asphyxia in Term Infants, U.S. Department of Health and Human Services, Public Health Service, National Institutes of Health, National Institute of Child Health and Human Development, [http://www.nichd.nih.gov/publications/pubs/acute/acute.cfm NIH Publication No. 96-3823], March 1996.</ref>]]


|-
Three-dimensional reconstruction of the lateral (top row) and medial (bottom row) surface of second trimester (13 to 21 week) brains to reveal the development of the Sylvian fissure or lateral sulcus (green arrow), the calcarine fissure (blue arrow), and the parieto-occipital sulcus (red arrow), respectively.
| <center>14</center>
|
| [[Tongue_Development|Tongue]] Week 14 to 15 - taste pores develop, mucous


|-
| <center>15</center>
| &nbsp;
| [http://embryology.med.unsw.edu.au/Notes/endocrine10.htm Pancreas ] glucagon detectable in fetal plasma


|-
[[File:Brain fissure development 02.jpg|600px]]
| <center>16</center>
| 14 cm
| [[Sensory_-_Hearing_and_Balance_Development|Hearing]] Week 16-24 - Centres of ossification appear in remaining cartilage of otic capsule form petrous portion of temporal bone. Continues to ossify to form mastoid process of temporal bone.


[http://embryology.med.unsw.edu.au/Notes/endocrine7.htm Pituitary ] adenohypophysis fully differentiated


[[Respiratory_System_Development|Respire]] Week 16 to 25 lung histology - canalicular
The images below are from a recent MRI study of fixed fetal brains at different weeks of development during the second trimester.{{#pmid:19339620|PMID19339620}}
<gallery>
File:Brain fissure development 02.jpg|Three-dimensional reconstruction of the lateral (top row) and medial (bottom row) surface of 13–21 week brains to reveal the development of the Sylvian fissure or lateral sulcus (green arrow), the calcarine fissure (blue arrow), and the parieto-occipital sulcus (red arrow), respectively.
File:Brain tract development 06.jpg|3D depiction of developmental white matter fibers. A lateral view of limbic tracts where pink fibers in 13, 15, and 19 week brains are the fornix and stria terminalis and purple fibers in the 19 week brains indicate the cingulum bundle.
File:Brain ventricles and ganglia development 02.jpg|Three-dimensional reconstruction of the basal ganglia and ganglionic eminence. Different colors represent different brain structures: whole brain (gray), ventricle (pink), ganglionic eminence (red), putamen and globus pallidus together (cyan), thalamus (yellow), and caudate nucleus (green).
File:Brain fissure development 03.jpg|Three-dimensional reconstruction of the lateral (top row) and medial (bottom row) surface of 13–21 week brains to reveal the development of the Sylvian or lateral fissure (green arrow).
</gallery>


[[Integumentary_System_Development|Skin]] 4 months - basal cell- proliferation generates folds in basement membrane; neural crest cells- (melanocytes) migrate into epithelium; embryonic connective tissue- differentiates into dermis, a loose ct layer over a dense ct layer. Beneath the dense ct layer is another loose ct layer that will form the subcutaneous layer. Ectoderm contributes to nails, hair follictles and glands. Nails form as thickening of ectoderm epidermis at the tips of fingers and toes. These form germinative cells of nail field. Cords of these cells extend into mesoderm forming epithelial columns. These form hair follocles, sebaceous and sweat glands.


primary follicles begin to form in the ovary and are characterized by an oocyte
:'''Links:''' [[Neural_System_-_Fetal|Neural System - Fetal]]


glandular urethra forms and skin folds present
==Second Trimester Timeline==
 
|-
| <center>17</center>
| &nbsp;
|
 
|-
| <center>18</center>
|
| [[Tongue_Development|Tongue]] Week 18 - substance P detected in dermal papillae, not in taste bud primordia
 
[[Integumentary_System_Development|Skin]] '''vernix caseosa covers skin
 
[http://embryology.med.unsw.edu.au/Notes/git8.htm Spleen] -SMA-positive reticulum cells increase in number and begin to form a reticular framework. [http://www.ncbi.nlm.nih.gov/pubmed/1925578 PMID: 1925578]
 
|-
| <center>19</center>
| &nbsp;
| &nbsp;
 
|-
| <center>20</center>
| &nbsp;
| [http://embryology.med.unsw.edu.au/Notes/endocrine7.htm Pituitary ] week 20 to 24  growth hormone levels peak, then decline


[[Integumentary_System_Development|Skin]] lanugo, skin hair
{{Second Trimester table01}}
 
[[Integumentary_System_Development|Skin]] 5 months - Hair growth initiated at base of cord, lateral outgrowths form associated sebaceous glands; Other cords elongate and coil to form sweat glands; Cords in mammary region branch as they elongate to form mammary glands.
 
[[Uterus_Development|Uterus Development]] uterine horn fimbrial development begins and continues after birth
|-
| <center>21</center>
| &nbsp;
| &nbsp;
 
|-
| <center>22</center>
| &nbsp;
| [http://embryology.med.unsw.edu.au/Notes/neuron.htm Neural]  brain cortical sulcation - sylvian fissure, interhemispheric fissure, callosal sulcus, parietooccipital fissure, and hippocampic fissures present([http://www.ncbi.nlm.nih.gov/pubmed/11158907 PMID:11158907]
 
[http://embryology.med.unsw.edu.au/Notes/git8.htm Spleen] - antigenic reticular framework diversity, T and B lymphocytes segregated in the framework [http://www.ncbi.nlm.nih.gov/pubmed/1925578 PMID: 1925578]
 
|-
| <center>23</center>
| &nbsp;
| &nbsp;
 
|-
| <center>24</center>
| &nbsp;
| [[Respiratory_System_Development|Respire]] Week 24 to 40 lung histology - terminal sac
 
Earliest potential survival expected if born
 
ovarian follicles can consist of growing oocytes surrounded by several layers of granulosa cells
 
|-
| <center>25</center>
| &nbsp;
| [[Respiratory_System_Development|Respire]] end month 6 alveolar cells type 2 appear and begin to secrete surfactant
 
|}


==References==
==References==
Line 148: Line 72:
'''Next''': [[Third Trimester]]
'''Next''': [[Third Trimester]]


{{Template:Glossary}}
{{Glossary}}


{{Template:Footer}}
{{Footer}}
[[Category:Human Embryo]] [[Category:Human Fetus]] [[Category:Second Trimester]]
[[Category:Human Embryo]] [[Category:Human Fetus]] [[Category:Second Trimester]]

Revision as of 09:24, 4 January 2019

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Introduction

Fetal size change

Ultrasound12wk 3D image2.jpg

Ultrasound Image of an early Fetus (12 week)


Fetal Links: fetal | Week 10 | Week 12 | second trimester | third trimester | fetal neural | Fetal Blood Sampling | fetal growth restriction | birth | birth weight | preterm birth | Developmental Origins of Health and Disease | macrosomia | BGD Practical | Medicine Lecture | Science Lecture | Lecture Movie | Category:Human Fetus | Category:Fetal
Historic Embryology  
1940 Fetus Physiology
Carnegie Fetal: 95 | 96 | 142 | 145 | 184 | 211 | 217 | 300 | 362 | 448 | 449 | 538 | 590 | 607 | 625 | 662 | 693 | 847 | 858 | 922 | 928 | 948 | 972 | 1318 | 1388 | 1455 | 1591 | 1597b | 1656 | 1686 | 2250a | 2250b | 3990 | 5652 | 6581 | 7218

Category:Second Trimester

Some Recent Findings

  • second trimester Serum Biomarker Screen for Fetal Aneuploidies as a Predictor of preterm birth: A Population-Based Study[1] "To determine the association between second-trimester serum Down syndrome screening (alpha-fetoprotein [AFP] free beta-human chorionic gonadotropin [b-hCG] unconjugated estriol [uE3]) and preterm birth and to create predictive models for preterm birth. Secondary analysis on a prospective database of pregnancies undergoing second-trimester screen with complete follow-up. The multiples of medians (MoM) of the biomarkers were compared between the group of term, preterm (< 37 weeks), early preterm (< 34 weeks), and very early preterm (< 32 weeks) delivery. Predictive models were developed based on adjusted MoMs and logistic regression and diagnostic performances in predicting preterm birth were determined. ...The second trimester Down syndrome screening could also be used as a tool of risk identification of preterm birth in the same test, without extra-effort and extra-cost."
  • Vitamin D - Lower vitamin D levels during the second trimester are associated with developing gestational diabetes mellitus: an observational cross-sectional study[2]

In this study, we aimed to compare serum 25(OH)D levels in women with and without gestational diabetes mellitus (GDM), and to identify the serum 25(OH)D levels associated with GDM. We recruited 40 women with GDM and 40 healthy pregnant women, aged 20-40 years and in the second trimester, at Gulhane Education and Research Hospital. We excluded women with chronic diseases, preeclampsia, pre-GDM, multiple pregnancies, and those taking medications related to calcium or vitamin D metabolism. We took anthropometric measurements and blood samples during the second trimester. Of the 80 pregnant women, pre-pregnancy body mass index was significantly higher among the GDM group than the healthy group (26.4 ± 5.73 kg/m2 vs. 22.6 ± 3.56 kg/m2, p = .001). Serum 25(OH)D levels in women with GDM were significantly lower than those in healthy women (16.8 ± 9.90 ng/mL vs. 20.9 ± 8.16 ng/mL, p = .016). The prevalence of severe vitamin D deficiency was as high as 72.5% among women in the GDM group, with a 1.74-fold increased risk of deficient status. Levels of 25(OH)D lower than a cutoff value of 14.0 ng/mL were determined to be related to GDM. These study results suggest that maternal vitamin D deficiency in mid-pregnancy is significantly associated with development of GDM."

More recent papers  
Mark Hill.jpg
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This table allows an automated computer search of the external PubMed database using the listed "Search term" text link.

  • This search now requires a manual link as the original PubMed extension has been disabled.
  • The displayed list of references do not reflect any editorial selection of material based on content or relevance.
  • References also appear on this list based upon the date of the actual page viewing.


References listed on the rest of the content page and the associated discussion page (listed under the publication year sub-headings) do include some editorial selection based upon both relevance and availability.

More? References | Discussion Page | Journal Searches | 2019 References | 2020 References

Search term: Second Trimester

Older papers  
These papers originally appeared in the Some Recent Findings table, but as that list grew in length have now been shuffled down to this collapsible table.

See also the Discussion Page for other references listed by year and References on this current page.

  • Review - Second trimester sonographic features of fetal chromosomal defects[3] "Advances in ultrasound technology have dramatically improved the detection of fetal chromosomal defects. Each chromosomal defect has its own syndromal pattern of detectable abnormalities prenataly. Most commonly detectable defects are Trisomies & Triploidies. Although only an invasive test can provide a definitive diagnosis, fetuses with major chromosomal abnormalities have either external or internal defects that can be recognized by detailed ultrasonographic examination at second trimester. These are defined as ultrasound markers for fetal aneuploidy. This article provides an overview and discussion on prenatal sonographic features that may suggest the presence of a common fetal chromosomal defect." ultrasound
  • Review - Second- and third-trimester biochemical and ultrasound markers predictive of ischemic placental disease.[4] "Ischemic placental disease is a recently coined term that describes the vascular insufficiency now believed to be an important etiologic factor in preeclampsia, intrauterine fetal growth restriction, and placental abruption. Given the increased risk for poor maternal and fetal outcomes, early prediction and prevention of this disorder is of significant clinical interest for many. In this article, we review the second- and third-trimester serum and ultrasound markers predictive of ischemic placental disease. Limited first-trimester data is also presented. While current studies report a statistical association between marker levels and various adverse perinatal outcomes, the observed diagnostic accuracy is below the threshold required for clinical utility. An exception to this generalization is uterine artery Doppler for the prediction of early-onset preeclampsia. Metabolomics is a relatively new analytic platform that holds promise as a first-trimester marker for the prediction of both early- and late-onset preeclampsia."

Neural Development

Timeline of events in Normal Human Neural Development[5]

Three-dimensional reconstruction of the lateral (top row) and medial (bottom row) surface of second trimester (13 to 21 week) brains to reveal the development of the Sylvian fissure or lateral sulcus (green arrow), the calcarine fissure (blue arrow), and the parieto-occipital sulcus (red arrow), respectively.


Brain fissure development 02.jpg


The images below are from a recent MRI study of fixed fetal brains at different weeks of development during the second trimester.[6]


Links: Neural System - Fetal

Second Trimester Timeline

Second Trimester (Clinical Week GA 14+)
Age (week)
Event
Fertilisation Age FA Gestational Age GA
12
14 Fetal head lateral.jpg Week 12 - CRL 85 mm, femur length 15 mm, biparietal diameter 25 mm

Hearing Week 12-16 - Capsule adjacent to membranous labrynth undegoes vacuolization to form a cavity (perilymphatic space) around membranous labrynth and fills with perilymph

Genital male and female external genital differences observable

Respiratory Month 3-6 - lungs appear glandular, end month 6 alveolar cells type 2 appear and begin to secrete surfactant

Tongue Week 12 - first differentiated epithelial cells (Type II and III)

Genital female genital canal (80 days) formed with absorption of the median septum

13
15 Tongue Week 12 to 13 - maximum synapses between cells and afferent nerve fibers

Hearing - Outer Ear Development Week 13 - Meatal plug disc-like, innermost surface in contact with the primordial malleus, contributes to the formation of the tympanic membrane.  

14
16 Tongue Week 14 to 15 - taste pores develop, mucous

Ovary Development 100 days - primary follicles present

Nail Development toenails appear

Head Development facial skeleton remodelling begins

15
17 Pancreas glucagon detectable in fetal plasma.

Spleen Week 15 -alpha-smooth muscle actin (alpha-SMA)-positive reticulum cells scattered around the arterioles. [7]

16
18 Fetal size change.jpg Hearing Week 16-24 - Centres of ossification appear in remaining cartilage of otic capsule form petrous portion of temporal bone. Continues to ossify to form mastoid process of temporal bone.

Pituitary adenohypophysis fully differentiated

Respiratory Week 16 to 25 lung histology - canalicular

Hearing - Outer Ear Development Week 16.5 - External auditory meatus is fully patent throughout its length, lumen is still narrow and curved.

Skin 4 months - basal cell- proliferation generates folds in basement membrane; neural crest cells- (melanocytes) migrate into epithelium; embryonic connective tissue- differentiates into dermis, a loose ct layer over a dense ct layer. Beneath the dense ct layer is another loose ct layer that will form the subcutaneous layer. Ectoderm contributes to nails, hair follictles and glands. Nails form as thickening of ectoderm epidermis at the tips of fingers and toes. These form germinative cells of nail field. Cords of these cells extend into mesoderm forming epithelial columns. These form hair follocles, sebaceous and sweat glands.

primary follicles begin to form in the ovary and are characterized by an oocyte

glandular urethra forms and skin folds present

17
19 Brain week 17 histology.jpg Neural - Brain development histology week 17
18
20 Bailey095.jpgTongue Week 18 - substance P detected in dermal papillae, not in taste bud primordia

Skin vernix caseosa covers skin

Spleen Week 18 - alpha-SMA-positive reticulum cells increase in number and began to form a reticular framework. An accumulation of T and B lymphocytes occurred within the framework, and a primitive white pulp was observed around the arterioles. [7]

Hearing - Outer Ear Development week 18 - External auditory meatus is already fully expanded to its complete form.

19
21  
20
22 Pituitary week 20 to 24 growth hormone levels peak, then decline

Skin lanugo, skin hair

Skin 5 months - Hair growth initiated at base of cord, lateral outgrowths form associated sebaceous glands; Other cords elongate and coil to form sweat glands; Cords in mammary region branch as they elongate to form mammary glands.

21
23  
22
24 Gray0038.jpg Neural brain cortical sulcation - sylvian fissure, interhemispheric fissure, callosal sulcus, parietooccipital fissure, and hippocampic fissures present[8]

Spleen - Week 22 - antigenic diversity of the reticular framework was observed, and T and B lymphocytes were segregated in the framework. T lymphocytes were sorted into the alpha-smooth muscle actin-positive reticular framework, and the periarteriolar lymphoid sheath (PALS) was formed around the arteriole. B lymphocytes aggregated in eccentric portions to the PALS and formed the lymph follicle (LF). The reticular framework of the LF was alpha-SMA-negative. [7]

23
25  
24
26 Respiratory Week 24 to 40 lung histology - terminal sac

Spleen Week 24 - marginal zone appeared in the alpha-smooth muscle actin-positive reticular framework around the white pulp.[7]

Earliest potential survival expected if born

ovarian follicles can consist of growing oocytes surrounded by several layers of granulosa cells

25
27 Respiratory end month 6 alveolar cells type 2 appear and begin to secrete surfactant

References

  1. Nunthapiwat S, Sekararithi R, Wanapirak C, Sirichotiyakul S, Tongprasert F, Srisupundit K, Luewan S & Tongsong T. (2019). Second Trimester Serum Biomarker Screen for Fetal Aneuploidies as a Predictor of Preterm Delivery: A Population-Based Study. Gynecol. Obstet. Invest. , , 1-8. PMID: 30602167 DOI.
  2. Ede G, Keskin U, Cemal Yenen M & Samur G. (2019). Lower vitamin D levels during the second trimester are associated with developing gestational diabetes mellitus: an observational cross-sectional study. Gynecol. Endocrinol. , , 1-4. PMID: 30599810 DOI.
  3. Akhter N & Chakraborty RK. (2014). Second trimester sonographic features of fetal chromosomal defects. Mymensingh Med J , 23, 412-6. PMID: 24858178
  4. Savasan ZA, Goncalves LF & Bahado-Singh RO. (2014). Second- and third-trimester biochemical and ultrasound markers predictive of ischemic placental disease. Semin. Perinatol. , 38, 167-76. PMID: 24836829 DOI.
  5. Report of the Workshop on Acute Perinatal Asphyxia in Term Infants, U.S. Department of Health and Human Services, Public Health Service, National Institutes of Health, National Institute of Child Health and Human Development, NIH Publication No. 96-3823, March 1996.
  6. Huang H, Xue R, Zhang J, Ren T, Richards LJ, Yarowsky P, Miller MI & Mori S. (2009). Anatomical characterization of human fetal brain development with diffusion tensor magnetic resonance imaging. J. Neurosci. , 29, 4263-73. PMID: 19339620 DOI.
  7. 7.0 7.1 7.2 7.3 <pubmed>19255788</pubmed>
  8. <pubmed>11158907</pubmed>

Search Pubmed: Second Trimester


Next: Third Trimester

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Cite this page: Hill, M.A. (2024, April 18) Embryology Second Trimester. Retrieved from https://embryology.med.unsw.edu.au/embryology/index.php/Second_Trimester

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