A Case of Female Pseudohermaphroditism with m llerian agenesis, urinary tract malformations, and imperforate anus.
- Author:
Yoon Sook KIM
;
Sang Sool KIM
;
Hyung Il KIM
;
Byung Jo MIN
;
Mi Young PARK
;
Kyung Soon LEE
- Publication Type:Case Report
- Keywords:
female pseudohermaphroditism;
m llerian agenesis;
urinary tract anomalies;
imperforate anus
- MeSH:
46, XX Disorders of Sex Development*;
Abortion, Therapeutic;
Anus, Imperforate*;
Autopsy;
Diagnosis;
Female*;
Fistula;
Genitalia;
Gestational Age;
Humans;
Lower Gastrointestinal Tract;
Multicystic Dysplastic Kidney;
Pregnancy;
Single Umbilical Artery;
Ureter;
Urinary Tract*
- From:Korean Journal of Obstetrics and Gynecology
2000;43(5):922-926
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
Special idiopathic female pseudohermaphroditism with urinary tract, m llerian duct, and lower gastrointestinal tract anomalies, in addition to masculinization of the external genitalia, is rare phenomenon. Masculinization of external genitalia and other anomalies occur in the absence of a recognized exposure to androgen or other teratogenic factors. We report a case of a female pseudohermaphroditism with m llerian agenesis, bilateral multicystic dysplastic kidney, urethral agenesis, left double ureter, rectovesical fistula, imperforate anus, single umbilical artery, detected after therapeutic abortion at 23+5 weeks of gestational age. The final diagnosis is based on autopsy.
