A case of male pseudohermaphroditism with an ahnormal triple analyte screening result

Filiz Avşar, Şelal Özmen, İ. Safa Kaya

  • Year : 1997
  • Vol : 13
  • Issue : 1
  •  Page : 67-68
Duı-ing a routine screening program for Down's syndrome. a patient was detected tü be in the high-risk group, because the human chorionic go-nadotropiıı level was high and the unconjugated est-riol level was low. An amniocentesis was perfrırmed and the karyotype was 46 XY. However, at deliver), the infant was found to be a male pse-udohermaphrodite due ta 313-01-1 dehydrogenase de-ficiency. We believe that the result of the triple analyte screening can not be related ta this enzyme deficienty.
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Description : None of the authors, any product mentioned in this article, does not have a material interest in the device or drug. Research, not supported by any external organization. grant full access to the primary data and, if requested by the magazine they agree to allow the examination of data.
A case of male pseudohermaphroditism with an ahnormal triple analyte screening result
, Vol. 13 (1)
Received : 13.10.1997, Accepted : 13.10.1997, Published Online : 13.10.2020
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ISSN:1017-6616;
E-ISSN:2149-8059;