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Disorder of Sex Development with 5alpha-reductase Deficiency in Identical Twins / 대한소아내분비학회지
Journal of Korean Society of Pediatric Endocrinology ; : 184-187, 2008.
Article in Korean | WPRIM | ID: wpr-97950
ABSTRACT
Children with abnormal sex development may present with ambiguous genitalia in the newborn period or lacking of secondary sexual characteristics in puberty. Clinicians should make a prompt and accurate diagnosis and counsel parents on therapeutic options to minimize or avoid medical and psychological complications. 5alpha-reductase deficiency is a rare autosomal recessive disorder of sex development caused by a mutation of the 5alpha-reductase type 2 gene. As a result, there is an abnormality in conversion of testosterone (T) to dihydrotestosterone (DHT) and children with 5alpha-reductase deficiency are born with ambiguous genitalia. Here, we report identical twins who presented with ambiguous genitalia with a 46,XY karyotype and were diagnosed as 5alpha-reductase deficiency.
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Full text: Available Index: WPRIM (Western Pacific) Main subject: Parents / Disorders of Sex Development / Dihydrotestosterone / Testosterone / Twins, Monozygotic / Puberty / Sexual Development / Karyotype Limits: Child / Humans / Infant, Newborn Language: Korean Journal: Journal of Korean Society of Pediatric Endocrinology Year: 2008 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Parents / Disorders of Sex Development / Dihydrotestosterone / Testosterone / Twins, Monozygotic / Puberty / Sexual Development / Karyotype Limits: Child / Humans / Infant, Newborn Language: Korean Journal: Journal of Korean Society of Pediatric Endocrinology Year: 2008 Type: Article