17,20-lyase : KMLE 의학 검색 엔진 - 의학사전, 의학용어, 의학약어, 의학논문, 약품/의약품 검색

KMLE 웹 용어 맞춤 검색 결과 : 1 페이지: 1

17,20-lyase deficiency	a disorder of steroidogenesis due to deficiency of 17α-hydroxyprogesterone aldolase, an enzyme activity normally catalyzing the conversion of C21 to C9 steroid hormones (androgens and estrogens); the result is a type of congenital adrenal hyperplasia (type V). Males are pseudohermaphroditic and both sexes remain sexually infantile. The enzyme activity is part of the enzyme steroid 17α-monooxygenase; see also 17α-hydroxylase deficiency and see table at hyperplasia. 출처: www.mercksource.com/pp/us/cns/cns_health_library.j...

17,20-lyase deficiency

a disorder of steroidogenesis due to deficiency of 17α-hydroxyprogesterone aldolase, an enzyme activity normally catalyzing the conversion of C21 to C9 steroid hormones (androgens and estrogens); the result is a type of congenital adrenal hyperplasia (type V). Males are pseudohermaphroditic and both sexes remain sexually infantile. The enzyme activity is part of the enzyme steroid 17α-monooxygenase; see also 17α-hydroxylase deficiency and see table at hyperplasia.

출처: www.mercksource.com/pp/us/cns/cns_health_library.j...