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Familial male pseudohermaphrodism with labial testes and partial feminization: endocrine studies and genetic aspects.

作者信息

LUBS H A, VILAR O, BERGENSTAL D M

出版信息

J Clin Endocrinol Metab. 1959 Sep;19:1110-20. doi: 10.1210/jcem-19-9-1110.

DOI:10.1210/jcem-19-9-1110
PMID:14418653
Abstract
摘要

相似文献

1
Familial male pseudohermaphrodism with labial testes and partial feminization: endocrine studies and genetic aspects.伴有阴唇睾丸及部分女性化的家族性男性假两性畸形：内分泌研究及遗传学方面
J Clin Endocrinol Metab. 1959 Sep;19:1110-20. doi: 10.1210/jcem-19-9-1110.
2
Endocrine studies in a case of male pseudohermaphrodism: testicular feminization.一例男性假两性畸形（睾丸女性化）的内分泌学研究
J Clin Endocrinol Metab. 1961 May;21:506-17. doi: 10.1210/jcem-21-5-506.
3
Pubertal feminization in a genetic male with testicular atrophy and normal urinary gonadotropin.一名患有睾丸萎缩且尿促性腺激素正常的遗传男性出现青春期女性化。
J Clin Endocrinol Metab. 1962 Aug;22:839-45. doi: 10.1210/jcem-22-8-839.
4
[Some remarks on the subject of the work of W. Taillard and A. Prader: "Genetic study of the total and partial syndrome of testicular feminization"].
J Genet Hum. 1959 Oct;8:199-207.
5
Familial primary amenorrhea due to testicular feminization: A human gene affecting sex differenctiation.因睾丸女性化导致的家族性原发性闭经：一个影响性别分化的人类基因。
Proc Soc Exp Biol Med. 1960 Jan;103:192-6. doi: 10.3181/00379727-103-25456.
6
[On a hereditary form of male pseudohermaphroditism ("testicular feminization")].论男性假两性畸形的一种遗传形式（“睾丸女性化”）
Geburtshilfe Frauenheilkd. 1959 Dec;19:1110-8.
7
Progestin binding in testes from three siblings with the syndrome of male pseudohermaphroditism with testicular feminization.三名患有男性假两性畸形伴睾丸女性化综合征的同胞兄弟的睾丸中的孕激素结合情况。
J Clin Endocrinol Metab. 1978 Jul;47(1):41-5. doi: 10.1210/jcem-47-1-41.
8
[On the problem of so-called testicular feminization (pseudohermaphroditism with the testes in the inguinal canal)].[关于所谓的睾丸女性化问题（腹股沟管内有睾丸的假两性畸形）]
Probl Endokrinol Gormonoter. 1963 Jan-Feb;9:99-102.
9
Male pseudohermaphrodism with female chromosomal complement.
J Clin Endocrinol Metab. 1961 Jun;21:727-31. doi: 10.1210/jcem-21-6-727.
10
[Familial male pseudohermaphrodism caused by testicular 17-ketosteroid-reductase deficiency].[睾丸17-酮类固醇还原酶缺乏所致的家族性男性假两性畸形]
Ann Endocrinol (Paris). 1973 Sep-Oct;34(5):461-75.

引用本文的文献

1
[ON THE CLINICAL ASPECTS AND HISTOPATHOLOGY OF PRIMARY MALE HYPOGONADISM. 1. NOSOLOGICAL CLASSIFICATION OF MALE HYPOGONADISM].[原发性男性性腺功能减退的临床特征与组织病理学。1. 男性性腺功能减退的疾病分类]
Arch Klin Exp Dermatol. 1963 Sep 2;217:117-48.
2
Secondary male hypogonadism and congenital ichthyosis: association of two rare genetic diseases.继发性男性性腺功能减退与先天性鱼鳞病：两种罕见遗传病的关联
Am J Hum Genet. 1960 Dec;12(4 Pt 1):440-7.
3
The androgen resistance syndromes: clinical and biochemical aspects.雄激素抵抗综合征：临床与生化方面
Eur J Pediatr. 1993;152 Suppl 2:S50-7. doi: 10.1007/BF02125440.
4
Cultured human skin fibroblasts: a model for the study of androgen action.培养的人皮肤成纤维细胞：雄激素作用研究的模型。
Mol Cell Biochem. 1981 Apr 13;36(1):3-22. doi: 10.1007/BF02354827.
5
Comments on some genetic abnormalities of sex determination and sex differentiation in Homo sapiens.关于人类性别决定和性别分化的一些遗传异常的评论
Eur J Pediatr. 1980 Mar;133(2):77-91. doi: 10.1007/BF00441575.
6
[Testicular feminization].[睾丸女性化]
Arch Klin Exp Dermatol. 1966;227(1):673-8. doi: 10.1007/BF00502917.
7
Male pseudohermaphroditism due to 17 alpha-hydroxylase deficiency.
J Clin Invest. 1970 Oct;49(10):1930-41. doi: 10.1172/JCI106412.
8
Clinical variations of testicular intersexuality in a family.一个家族中睾丸性两性畸形的临床变异
J Med Genet. 1974 Sep;11(3):267-70. doi: 10.1136/jmg.11.3.267.
9
["Transsexualism" in testicular feminization].睾丸女性化中的“易性癖”
Klin Wochenschr. 1972 Jul 15;50(14):696-701. doi: 10.1007/BF01495528.
10
[Intersex types which are difficult to classify. I. Familial masculine pseudohermaphroditism with disproportioned virilization and chromosomal aberration].难以分类的两性畸形类型。I. 伴有不成比例的男性化和染色体畸变的家族性男性假两性畸形
Klin Wochenschr. 1970 Mar 15;48(6):341-6. doi: 10.1007/BF01484860.