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Hereditary Male Pseudohermaphroditism
Clinics in Obstetrics and Gynaecology, 1978SUMMARY The anatomical, genetic, and endocrine features of hereditary male pseudohermaphroditism are summarized in Table 1. On the basis of these characteristics, it is usually possible in the postpubertal state to arrive at a satisfactory diagnosis, recognizing certain limitations. For example, the family history may be uninformative.
J E, Griffin, J D, Wilson
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FAMILIAL MALE PSEUDOHERMAPHRODITISM
Acta Endocrinologica, 1965ABSTRACT A family is presented in which all males of the second generation died at birth, and in which two out of four individuals of the third generation exhibited ambiguous external genitalia. All members of the third generation, one brother and one sister in one sibship, and two brothers in another sibship, were studied from both a clinical ...
K, BOCZKOWSKI, J, TETER
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Familial Male Pseudohermaphroditism
Human Heredity, 1972Four families comprising eight propositi presenting different types of familial male pseudoherma phroditism have been studied genealogically.
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[Female pseudohermaphroditism].
Presse medicale (Paris, France : 1983), 1994Contrary to what is observed in true hermaphroditism and in male pseudo-hermaphroditism, there is no erroneous transmission of the genetic gonadal differentiation programme in female pseudohermaphroditism. All that has happened is virilization of the urogenital sinus and external genitalia in a foetus exposed to exo- or endogenous androgens.
H N, Minh, J, Belaisch, A, Smadja
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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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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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FAMILIAL MALE PSEUDOHERMAPHRODITISM
Medical Journal of Australia, 1970A C, Walker, E M, Stack, W A, Horsfall
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