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Results 11 - 18 of 18 for Male hypogonadism
  1. Gordon Holmes syndrome 
    ... production of hormones that direct sexual development (hypogonadotropic hypogonadism). Many affected individuals have a delay in development of the typical signs of puberty, such as the growth of facial hair and deepening of the voice in males, and the start of monthly periods (menstruation) and ...
    https://medlineplus.gov/genetics/condition/gordon-holmes-syndrome - Genetics
  2. Boucher-Neuhäuser syndrome 
    ... key feature of Boucher-Neuhäuser syndrome is hypogonadotropic ... of the voice in males, and the start of monthly periods (menstruation) and ...
    https://medlineplus.gov/.../condition/boucher-neuhauser-syndrome - Genetics
  3. 48,XXXY syndrome 
    48,XXXY syndrome is a chromosomal condition in boys and men that causes intellectual disability, developmental delays, physical differences, and an inability ...
    https://medlineplus.gov/genetics/condition/48xxxy-syndrome - Genetics
  4. Klinefelter syndrome 
    ... Nieschlag E. Klinefelter syndrome: the commonest form of hypogonadism, but often ... in Males with Sex Chromosome Aneuploidy: XXY/Klinefelter Syndrome, XYY, ...
    https://medlineplus.gov/genetics/condition/klinefelter-syndrome - Genetics
  5. Hartsfield syndrome 
    ... leading to slow or delayed growth; and hypogonadotropic hypogonadism, which ... Hartsfield syndrome is caused by mutations in the ...
    https://medlineplus.gov/genetics/condition/hartsfield-syndrome - Genetics
  6. Prader-Willi syndrome 
    Prader-Willi syndrome is a complex genetic condition that affects many parts of the body. In infancy, this condition is characterized by weak muscle tone (hypotonia), ...
    https://medlineplus.gov/genetics/condition/prader-willi-syndrome - Genetics
  7. SOX2 anophthalmia syndrome 
    ... have been described in affected individuals, especially males. Male genital abnormalities include ... D, Dattani MT. The role of SOX2 in hypogonadotropic hypogonadism. Sex Dev. 2008;2(4-5):194-9. ...
    https://medlineplus.gov/.../condition/sox2-anophthalmia-syndrome - Genetics
  8. 49,XXXXY syndrome 
    49,XXXXY syndrome is a chromosomal condition that causes intellectual disabilities, developmental delays, changes in sex characteristics and other physical ...
    https://medlineplus.gov/genetics/condition/49xxxxy-syndrome - Genetics
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