Gonadal agenesis 46,XX associated with the atypical form of Rokitansky syndrome

Fertility and Sterility

Volumn 77, Issue 1, 2002, Pages 185-187

  Gorgojo, Juan José ^a   Almodóvar, Francisca ^a   López, Elena ^a   Donnay, Sergio ^a  

^a HOSPITAL UNIVERSITARIO FUNDACIÓN ALCORCÓN   (Spain)

Author keywords

Gonadal agenesis; M llerian agenesis; Primary hypothyroidism; Renal agenesis; Rokitansky syndrome

Indexed keywords

ADOLESCENT; AMENORRHEA; ANALYTIC METHOD; ARTICLE; BREAST DEVELOPMENT; CASE REPORT; CLINICAL FEATURE; DISEASE ASSOCIATION; ENDOCRINE FUNCTION TEST; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GONADAL AGENESIS; GONADOTROPIN BLOOD LEVEL; GYNECOLOGICAL EXAMINATION; HUMAN; HYPOTHYROIDISM; INTRAVENOUS UROGRAPHY; KARYOTYPE; LABORATORY TEST; LAPAROSCOPY; PHYSICAL EXAMINATION; PRIORITY JOURNAL; ROKITANSKY SYNDROME; SKELETON MALFORMATION; SPAIN; ULTRASOUND; UROGENITAL TRACT MALFORMATION; UROGRAPHY; Y CHROMOSOME;

ABNORMALITIES, MULTIPLE; ADOLESCENT; AMENORRHEA; CHROMOSOME MAPPING; FEMALE; GONADAL DYSGENESIS; HUMANS; KIDNEY; SYNDROME;

EID: 0036155897     PISSN: 00150282     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0015-0282(01)02943-0     Document Type: Article

References (4)

1. Mayer-Rokitansky-Küster-Hauser syndrome: Distinction between two forms based on excretory urographic, sonographic, and laparoscopic findings
2. Vaginal agenesis (Mayer-Rokitansky-Küster-Hauser syndrome) associated with the N314D mutation of galactose-1-phosphate uridyl transferase (GALT)
3. An XX female with sexual infantilism, absent gonads and lack of Müllerian ducts
4. Gonadal dysgenesis and Rokitansky syndrome. A case report