Androgen insensitivity syndrome screening: Difference between revisions
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==Screening== | ==Screening== | ||
* The diagnosis of AIS is mostly made postnatally. But, in a study which diagnosed mid-second trimester fetus with thick NT/NF and short limbs likely to be AIS. Hence, appearance of fetal sex on ultrasound should be compared with genetic sex. <ref name="pmid17605153">{{cite journal |vauthors=Yalinkaya A, Yayla M, Erdemoglu M |title=Prenatal diagnosis of a fetus with androgen insensitivity syndrome (AIS) |journal=Prenat. Diagn. |volume=27 |issue=9 |pages=856–7 |year=2007 |pmid=17605153 |doi=10.1002/pd.1747 |url=}}</ref> | |||
==References== | ==References== |
Revision as of 14:53, 11 July 2017
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Overview
Screening
- The diagnosis of AIS is mostly made postnatally. But, in a study which diagnosed mid-second trimester fetus with thick NT/NF and short limbs likely to be AIS. Hence, appearance of fetal sex on ultrasound should be compared with genetic sex. [1]
References
- ↑ Yalinkaya A, Yayla M, Erdemoglu M (2007). "Prenatal diagnosis of a fetus with androgen insensitivity syndrome (AIS)". Prenat. Diagn. 27 (9): 856–7. doi:10.1002/pd.1747. PMID 17605153.