Congenital adrenal hyperplasia: Surgical considerations required to repair a 46,XX patient raised as a boy

Journal of Pediatric Surgery

Volumn 38, Issue 8, 2003, Pages 1269-1273

  Dasgupta, Roshni ^a   Schnitzer, J Jay ^a   Hendren, W Hardy ^b   Donahoe, Patricia K ^a  

^a MASSACHUSETTS GENERAL HOSPITAL   (United States)

^b BOSTON CHILDREN S HOSPITAL   (United States)

Author keywords

Congenital adrenal hyperplasia; Genital ambiguity

Indexed keywords

ANDROGEN; HORMONE PRECURSOR; HYDROCORTISONE; STEROID 21 MONOOXYGENASE; TESTOSTERONE;

ADOLESCENT; ANDROGEN BLOOD LEVEL; ANDROGEN SYNTHESIS; ARTICLE; CASE REPORT; CONGENITAL ADRENAL HYPERPLASIA; CONSANGUINEOUS MARRIAGE; DISEASE ASSOCIATION; GENETIC ANALYSIS; GENITAL MALFORMATION; HETEROZYGOTE; HORMONAL THERAPY; HORMONE SUBSTITUTION; HUMAN; HYDROCORTISONE BLOOD LEVEL; HYPOSPADIAS; IMPLANTATION; KARYOTYPE 46,XX; MALE; MUELLERIAN DUCT; PAKISTAN; PENIS DISEASE; PRIORITY JOURNAL; SCROTUM DISORDER; STEROID 21 MONOOXYGENASE DEFICIENCY; SURGICAL TECHNIQUE; TREATMENT PLANNING; UROGENITAL SINUS; VIRILIZATION;

EID: 0042861691     PISSN: 00223468     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0022-3468(03)00287-2     Document Type: Article

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