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A male pseudohermaphrodite.

South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde, 1968
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Dysgenetic Male Pseudohermaphroditism

Journal of Urology, 1978
Dysgenetic male pseudohermaphroditism is a disorder of sexual differentiation in which patients present with bilateral dysgenetic testes, persistent müllerian structures, cryptorchidism and inadequate virilization. There were 10 patients with this syndrome seen at our hospital between 1956 and 1976.
J, Rajfer, G, Mendelsohn, J, Arnheim, R D, Jeffs, P C, Walsh   +4 more
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Familial male pseudohermaphroditism

The Indian Journal of Pediatrics, 1997
Familial male pseudohermaphroditism (MPH) due to 17,20-desmolase deficiency is rare. Here we present two siblings with MPH possibly due to 17,20-desmolase deficiency. The first patient presented with unambiguous female external genitalia and hypergonadotrophic hypogonadism. Chromosomal analysis revealed 46 XY.
A C, Ammini, D C, Sharma, R, Gupta, I, Mohapatra, K, Kucheria, A, Kriplani, D, Takkar, D K, Mitra, M, Vijayaraghavan   +8 more
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Dysgenetic male pseudohermaphroditism

Orvosi Hetilap, 2012
The authors report a case of a dysgenetic male pseudohermaphroditism with a 45,X/46,XY karyotype in a mosaic form, which was diagnosed in an infant. The one-week-old infant was evaluated because of proximal hypospadias and retention of the right testis. The results of hormonal tests were the followings: serum FSH 5.2 mU/ml; LH: 2.0 mU/ml; testosterone:
László, Ságodi, Janka, Jakab, Akos, Kiss, Erzsébet, Ladányi, Erzsébet, Balogh, Anikó, Ujfalusi, Judit, Papp, Tímea, Megyeri, Judit, Kovács   +8 more
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Hereditary Male Pseudohermaphroditism

Clinics in Obstetrics and Gynaecology, 1978
SUMMARY 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, 1965
ABSTRACT 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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Incomplete Male Pseudohermaphroditism

New England Journal of Medicine, 1974
exaly   +4 more sources