scholarly journals FEMALE PSEUDOHERMAPHRODITISM

10.4081/346 ◽  
2009 ◽  
Vol 1 (1) ◽  
Author(s):  
AL. Bulotta ◽  
C. Varetti ◽  
F. Ferrara ◽  
G. Giannotti ◽  
G. Di Maggio ◽  
...  
Keyword(s):  
Female Pseudohermaphroditism

Danazol May Cause Female Pseudohermaphroditism

1981 ◽  
Vol 35 (2) ◽  
pp. 230-231 ◽  
Author(s):  
Stephen C. Duck ◽  
K. Paul Katayama
Keyword(s):  
Female Pseudohermaphroditism

FEMALE PSEUDOHERMAPHRODITISM DUE TO PROGESTOGENS

The Lancet ◽  
1960 ◽  
Vol 276 (7147) ◽  
pp. 438-439 ◽  
Author(s):  
P.E. Mortimer
Keyword(s):  
Female Pseudohermaphroditism

Female Pseudohermaphroditism

2009 ◽  
pp. 650-650
Author(s):  
Robert J. Desnick ◽  
Orlando Guntinas-Lichius ◽  
George W. Padberg ◽  
Gustav Schonfeld ◽  
Xiaobo Lin ◽  
...  
Keyword(s):  
Female Pseudohermaphroditism

Female pseudohermaphroditism associated with cloacal anomalies: Faulty differentiation in the caudal developmental field

2001 ◽  
Vol 36 (7) ◽  
pp. 1-3 ◽  
Author(s):  
Rajiv Chadha ◽  
Sunil K. Kothari ◽  
Ujjwal S. Tanwar ◽  
Sanjay Gupta
Keyword(s):  
Female Pseudohermaphroditism ◽  
Cloacal Anomalies

Sindrome adrenogenitale ereditaria (Pseudoermafroditismo femminile) Effetti della surrenectomia parziale

1959 ◽  
Vol 8 (3) ◽  
pp. 279-298
Author(s):  
I. Gatto ◽  
A. La Grutta
Keyword(s):  
Adrenal Glands ◽  
Female Pseudohermaphroditism ◽  
Secondary Sexual Characters ◽  
Male Type ◽  
Early Appearance ◽  
Recessive Type ◽  
Secondary Sexual

SUMMARYIn two sisters a female pseudohermaphroditism was found, due to constitutional hyperplasia of the adrenal glands. The typical alterations of external genitals already present at birth were associated with an early appearance of secondary sexual characters of the male type and exaggerated expulsion of the 17 urinary ketosteroids.There were signs of a deficiency of mineral-and glycogen-active hormones, but they were not such as to give clinic manifestations.In one of the patients the amputation of one third of both adrenal glands caused a transitory improvement.The familiality observed in these cases leads the authors to assume a hereditary transmission of the recessive type.

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