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Complete Androgen Insensitivity Syndrome in Three Sisters
被引:0
|作者:
Verim, Levent
[1
]
机构:
[1] Haydarpasa Numune Training Hosp, Dept Urol, Istanbul, Turkey
关键词:
Disorder of Sexual Development;
46 XY Female;
Androgen Receptor;
Mutation;
Infertility;
D O I:
暂无
中图分类号:
R71 [妇产科学];
学科分类号:
100211 ;
摘要:
Disorders of sexual development (DSD) are congenital anomalies due to atypical development of chromosomes, gonads and anatomy. Complete androgen insensitivity syndrome (CAIS), also known as testicular feminization (TF) is a rare DSD disease. The majority of CAIS patients apply to hospital with the complaint of primary amenorrhea or infertility. Given that CAIS patients are all phenotypically female while having 46, XY karyotypes, CAIS diagnosis should be disclosed in an age-appropriate manner preferably by a mental health professional. Cases are reported here for three 46XY siblings consistent with CAIS.
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页码:353 / 356
页数:4
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