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Kindler Syndrome: A Case Report From a Developing Country. [PDF]
Clin Case RepHraib M, Ali Deeb C, Dib T, Baddour R.
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Artificially Induced Female Pseudohermaphroditism
New England Journal of Medicine, 1958"EXPERIMENTAL intersexes have been produced by the administration of androgens to the gravid mouse, rat, hamster, ground hog, porcupine, guinea pig, rabbit and monkey. Recently, this experiment was unwittingly reproduced in the human being, and female pseudohermaphrodites born of mothers treated with androgens during pregnancy have been reported.
exaly +3 more sources
Journal of Urology, 1942
Of several classifications of patients with hermaphroditism that have been proposed to date, the most lucid and self-explanatory one is that of McCahey, 1 which is as follows: group 1, male pseudohermaphrodites without mullerian derivatives; group 2, female pseudohermaphrodites; group 3, true hermaphrodites; group 4, male pseudohermaphrodites with ...
Ira R. Sisk, Philip M. Cornwell
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Of several classifications of patients with hermaphroditism that have been proposed to date, the most lucid and self-explanatory one is that of McCahey, 1 which is as follows: group 1, male pseudohermaphrodites without mullerian derivatives; group 2, female pseudohermaphrodites; group 3, true hermaphrodites; group 4, male pseudohermaphrodites with ...
Ira R. Sisk, Philip M. Cornwell
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Dysgenetic Male Pseudohermaphroditism
Journal of Urology, 1978Dysgenetic 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 +4 more
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Familial male pseudohermaphroditism
The Indian Journal of Pediatrics, 1997Familial 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 +8 more
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Dysgenetic male pseudohermaphroditism
Orvosi Hetilap, 2012The 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 +8 more
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