Skip navigation

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you’ve safely connected to the .gov website. Share sensitive information only on official, secure websites.

Results 1 - 10 of 28 for Male pseudohermaphroditism
  1. ... reductase type 2 gene (SRD5A2) leads to severe male pseudohermaphroditism in a Turkish family. Urology. 2005 Aug;66( ...
  2. ... a female, but the genetic makeup of a male. PAIS is a type of androgen insensitivity syndrome (AIS) . AIS is one of the conditions that are described as disorders of sex development (DSD).
  3. Persistent Müllerian duct syndrome is a disorder of sexual development that affects males. Males with this disorder have normal male reproductive organs, though ...
  4. ... the luteinizing hormone/chorionic gonadotropin receptor gene cause male pseudohermaphroditism. PLoS Med. 2008 Apr 22;5(4):e88. ... with a novel missense mutation of LHCGR cause male pseudohermaphroditism. Hum Mutat. 2009 Sep;30(9):E855-65. ...
  5. ... the luteinizing hormone/chorionic gonadotropin receptor gene cause male pseudohermaphroditism. PLoS Med. 2008 Apr 22;5(4):e88. ... with a novel missense mutation of LHCGR cause male pseudohermaphroditism. Hum Mutat. 2009 Sep;30(9):E855-65. ...
  6. Campomelic dysplasia From the National Institutes of Health (Genetic and Rare Diseases Information Center)  
    Genetic and Rare Diseases Information Center ... From the National Institutes of Health ... Birth Defects/Specifics ... Birth Defects ... Bone Diseases/Children ... Bone Diseases
  7. ... XX testicular disorder/difference of sex development XX male syndrome Genetic Testing Registry: 46,XX testicular disorder of sex development 46,XX testicular disorder of sex development Disease ...
  8. ... KSR deficiency Neutral 17-beta-hydroxysteroid oxidoreductase deficiency Pseudohermaphroditism, male, with gynecomastia Testosterone 17-beta-dehydrogenase deficiency 17- ...
  9. ... in the TSPYL1 gene associated with 46,XY disorder of sex development and male infertility. Fertil Steril. 2009 Oct;92(4):1347- ...
  10. ... have external genitalia that do not look clearly male or clearly female or other changes in the genitals and reproductive organs.Some people with the features of 46,XY disorder of sex development caused by DHH gene variants also have nerve ...
previous · 1 · 2 · 3 · next