[与17-α羟化酶缺乏相关的男性假两性畸形]
[Male pseudohermaphroditism related to 17-alpha hydroxylase deficiency].
作者信息
Liotta A, Cammarata M, Corsello G, Ferrara D, Giuffrè L
机构信息
Clinica Pediatrica I, Università di Palermo, Italia.
出版信息
Pediatr Med Chir. 1987 May-Jun;9(3):309-10.
PMID:2823235
Abstract
A case of male pseudohermaphroditism with adrenal failure and female external genitalia is described. The hormonal pattern and the clinical evolution of the patient are compatible to a partial 17 alpha hydroxylase deficiency.
摘要
描述了一例患有肾上腺功能衰竭且具有女性外生殖器的男性假两性畸形病例。患者的激素模式和临床病程与部分17α-羟化酶缺乏症相符。
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