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Familial incomplete male pseudohermaphroditism, type 2. Decreased dihydrotestosterone formation in pseudovaginal perineoscrotal hypospadias.

作者信息

Walsh P C, Madden J D, Harrod M J, Goldstein J L, MacDonald P C, Wilson J D

出版信息

N Engl J Med. 1974 Oct 31;291(18):944-9. doi: 10.1056/NEJM197410312911806.

DOI:10.1056/NEJM197410312911806
PMID:4413434
Abstract
摘要

相似文献

1
Familial incomplete male pseudohermaphroditism, type 2. Decreased dihydrotestosterone formation in pseudovaginal perineoscrotal hypospadias.2型家族性不完全性男性假两性畸形。假性阴道会阴阴囊型尿道下裂中双氢睾酮生成减少。
N Engl J Med. 1974 Oct 31;291(18):944-9. doi: 10.1056/NEJM197410312911806.
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Familial male pseudohermaphroditism without gynecomastia due to deficient testicular 17-ketosteroid reductase activity.由于睾丸17-酮类固醇还原酶活性缺乏导致的无男子女性型乳房的家族性男性假两性畸形。
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Familial incomplete male pseudohermaphroditism, type 1. Evidence for androgen resistance and variable clinical manifestations in a family with the Reifenstein syndrome.1型家族性不完全性男性假两性畸形。Reifenstein综合征家族中雄激素抵抗及可变临床表现的证据。
N Engl J Med. 1974 May 16;290(20):1097-103. doi: 10.1056/NEJM197405162902001.
4
Familial male pseudohermaphroditism with incomplete virilization.
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Editorial: His and hers.社论：他的和她的。
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Phenotypic classification of male pseudohermaphroditism due to steroid 5 alpha-reductase 2 deficiency.由类固醇5α-还原酶2缺乏引起的男性假两性畸形的表型分类。
Am J Med Genet. 1996 May 3;63(1):223-30. doi: 10.1002/(SICI)1096-8628(19960503)63:1<223::AID-AJMG39>3.0.CO;2-O.
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Male pseudohermaphroditism due to 5 alpha-reductase deficiency. Ultrastructure of the gonads.
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Molecular diagnosis of 5alpha-reductase-2 gene mutation in two Indian families with male pseudohermaphroditism.两个患有男性假两性畸形的印度家庭中5α-还原酶-2基因突变的分子诊断
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Male pseudohermaphroditism due to testicular 17 -hydroxysteroid dehydrogenase deficiency.
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