- A case of male Pseudohermaphroditism due to 17alpha-Hydroxylase Deficiency
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Kim JH, Choi SY, Kim JH, Kim JH, Rha JG, Kang CS
- KMID: 2260800
- Korean J Obstet Gynecol.
- 1997 Apr;40(4):896-901.
A 21-year-old phenotypic female with 46,XY genotype presented with primary amenorrhea, headache, absence of secondary sex characteristics, and hypertension.Further evaluation confirmed male pseudohermaphroditism having no nterus and adnexase.After basic hormonal... -
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