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: Presymptomatic diagnosis of X-linked adrenal hypoplasia congenita by analysis of DAX1.
    Author: Achermann JC, Silverman BL, Habiby RL, Jameson JL.
    Journal: J Pediatr; 2000 Dec; 137(6):878-81. PubMed ID: 11113848.
    Abstract:
    A novel DAX1 mutation (L381H) was discovered in the asymptomatic 8-month-old brother of a boy with primary adrenal failure. The infant had impaired adrenal reserve despite normal basal adrenal steroid concentrations. This case highlights the value of genetic testing in children at risk of the development of X-linked adrenal hypoplasia congenita before the onset of a potentially life-threatening adrenal crisis.
    [Abstract] [Full Text] [Related] [New Search]