Prenatal diagnosis of a fetus with androgen insensitivity syndrome (AIS)

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dc.contributor.authorYalınkaya, Ahmet
dc.contributor.authorYayla, Murat
dc.contributor.authorErdemoğlu, Mahmut
dc.date.accessioned2024-04-24T15:59:30Z
dc.date.available2024-04-24T15:59:30Z
dc.date.issued2007
dc.departmentDicle Üniversitesi, Tıp Fakültesi, Cerrahi Tıp Bilimleri Bölümü, Kadın Hastalıkları ve Cerrahi Ana Bilim Dalıen_US
dc.description.abstractObjective The aim of this study is to describe a fetus with androgen insensitivity syndrome diagnosed at mid-second trimester. Case and Methods Nuchal translucency was measured thick and double test was found higher. The patient referred to our center at 16(th) weeks of gestation. Fetal ultrasound examination and amniocentesis was performed. Results The nuchal translucency (NT) of fetus in present pregnancy was measured approximately 10 mm at 13 weeks and Down syndrome risk was calculated I in 10 by double test. On ultrasound examination; thick nuchal fold (NF) and short fetal limbs were found, and the fetus was seen a female and amniocentesis was performed. Three weeks later the fetal karyotype was reported normal as 46,XY. Thereupon the fetus reexamined for 2D and 4D ultrasound, and confirmed previous findings. The fetus was terminated at 19(th) weeks and seen a female phenotype. The fetal gonads removed in abdomen and testicles confirmed histopatologically. Conclusion In generally, diagnosis of AIS is most made postnatally. This is the second case in English literature, which diagnosed mid-second trimester. In this situation, the fetus with thick NT/NF and short limbs may be AIS, therefore appearance of fetal sex on ultrasound should be compared with genetic sex.en_US
dc.identifier.citationYalınkaya, A., Yayla, M. ve Erdemoğlu, M. (2007). Prenatal diagnosis of a fetus with androgen insensitivity syndrome (AIS). Prenatal Diagnosis, 27(9), 856-857.
dc.identifier.doi10.1002/pd.1747
dc.identifier.endpage857en_US
dc.identifier.issn0197-3851
dc.identifier.issue9en_US
dc.identifier.pmid17605153
dc.identifier.scopus2-s2.0-34548758434
dc.identifier.scopusqualityQ1
dc.identifier.startpage856en_US
dc.identifier.urihttps://doi.org/10.1002/pd.1747
dc.identifier.urihttps://hdl.handle.net/11468/14112
dc.identifier.urihttps://obgyn.onlinelibrary.wiley.com/doi/10.1002/pd.1747
dc.identifier.volume27en_US
dc.identifier.wosWOS:000249713000013
dc.identifier.wosqualityQ3
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.institutionauthorYalınkaya, Ahmet
dc.institutionauthorYayla, Murat
dc.institutionauthorErdemoğlu, Mahmut
dc.language.isoenen_US
dc.publisherJohn Wiley & Sons Ltden_US
dc.relation.ispartofPrenatal Diagnosis
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectPrenatalen_US
dc.subjectDiagnosisen_US
dc.subjectAndrogenen_US
dc.subjectInsensitivityen_US
dc.subjectSyndromeen_US
dc.titlePrenatal diagnosis of a fetus with androgen insensitivity syndrome (AIS)en_US
dc.titlePrenatal diagnosis of a fetus with androgen insensitivity syndrome (AIS)
dc.typeArticleen_US

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