A Case of Female Pseudohermaphroditism with m llerian agenesis, urinary tract malformations, and imperforate anus / 대한산부인과학회잡지
Korean Journal of Obstetrics and Gynecology
;
: 922-926, 2000.
Article
in Korean
| WPRIM
| ID: wpr-88152
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.
Full text:
Available
Index:
WPRIM (Western Pacific)
Main subject:
Anus, Imperforate
/
Autopsy
/
Ureter
/
Urinary Tract
/
Gestational Age
/
Abortion, Therapeutic
/
Multicystic Dysplastic Kidney
/
Lower Gastrointestinal Tract
/
Diagnosis
/
46, XX Disorders of Sex Development
Type of study:
Diagnostic study
Limits:
Female
/
Humans
/
Pregnancy
Language:
Korean
Journal:
Korean Journal of Obstetrics and Gynecology
Year:
2000
Type:
Article
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