These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


PUBMED FOR HANDHELDS

Search MEDLINE/PubMed


  • Title: The Aarskog syndrome in a large family, suggestive for autosomal dominant inheritance.
    Author: van de Vooren MJ, Niermeijer MF, Hoogeboom AJ.
    Journal: Clin Genet; 1983 Dec; 24(6):439-45. PubMed ID: 6652957.
    Abstract:
    A large family in which the Aarskog syndrome is transmitted in three generations was studied. In affected males, a large variability of expression was observed, while females show minor signs only. However it is sometimes possible to identify individual females as carriers. The observation of male to male transmission and the absence of symptoms in some daughters of affected male persons suggest a sex-influenced autosomal inheritance in this family. This may suggest heterogeneity in the Aarskog syndrome, since in most families described an X-linked recessive mode of inheritance was indicated.
    [Abstract] [Full Text] [Related] [New Search]