Results 171 to 180 of about 8,597 (215)

Male Pseudohermaphroditism

Pediatrics In Review, 1982
Male pseudohermaphroditism is the condition of incomplete male differentiation of the external genitalia in an individual with a Y chromosome. The gonads of the male pseudohermaphrodite, when present, are either streak gonads or testes. A wide range of disorders and phenotypic presentations are encompassed by the term male ...
Donna J. Levy, Lenore S. Levine, Maria I. New   +2 more
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Nongenetic Male Pseudohermaphroditism

New England Journal of Medicine, 2002
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Familial Male Pseudohermaphroditism

Human Heredity, 1972
Four families comprising eight propositi presenting different types of familial male pseudoherma phroditism have been studied genealogically.
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Male pseudohermaphroditism.

Annales d'endocrinologie, 1981
The abnormalities of male sex differentiation are relevant from chromosomal abnormalities, male differentiation with inappropriate karyotype, true hermophroditism and male pseudohermaphroditism (MPH). We define MPH as incomplete masculinization of the external genitalia in subjects with normal 46 XY karyotype.
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Male Pseudohermaphroditism and Chromosomal Mosaicism

Archives of Pediatrics & Adolescent Medicine, 1962
The following is a case report on the subject of chromosomal mosaicism and male pseudohermaphroditism. Report of a Case The patient was a Negro boy who weighed 3,020 gm. at birth and appeared entirely normal with the exception of the external ears and genitalia. His mother was 42, the father 47 years old. Consanguinity was denied.
J, WARKANY, E H, CHU, E, KAUDER
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FAMILIAL MALE PSEUDOHERMAPHRODITISM

Medical Journal of Australia, 1970
A C, Walker, E M, Stack, W A, Horsfall
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[Dysgenetic male pseudohermaphroditism].

Acta medica portuguesa, 2002
Dysgenetic male pseudohermaphroditism is the result of a defect of testis development that encompasses a large clinical heterogeneity. It is characterized by bilateral dysgenetic testis, absence of mullerian regression, ambiguous genitalia and/or stigmata of Turner's syndrome in the majority of the cases.
E, Proença, S, Freitas, M, Fonseca, S, Figueiredo, C, Rodrigues   +4 more
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Surgical approach to male pseudohermaphroditism

European Journal of Pediatrics, 1993
Male pseudohermaphroditism (MPH) is defined as incomplete masculinization in patients with normal male karyotype (XY) and testicular histology. MPH encompasses a spectrum of female to male phenotypes and presents both diagnostic and technical challenges to the surgeon.
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[Male pseudohermaphroditism].

Nihon rinsho. Japanese journal of clinical medicine, 1995
Male pseudohermaphroditism is a condition of sex differentiation disorders in which the gonads are tests, but the genital ducts and/or external genitalia are incompletely masculinized. This syndrome is caused by a failure of the sequential process in embryonal development of the testis. In the presence of functioning testis the Müllerian ducts regress,
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MALE PSEUDOHERMAPHRODITISM

Obstetrical & Gynecological Survey, 1955
O. ALVES DE LIMA, K. M. RUDOLPH, A. GASTIM   +2 more
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