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

PUBMED FOR HANDHELDS

Search MEDLINE/PubMed

  • Title: Meckel Gruber Syndrome--a case report.
    Author: Desai SR, Wader JV.
    Journal: Indian J Pathol Microbiol; 2004 Jul; 47(3):430-2. PubMed ID: 16295449.
    Abstract:
    Meckel Gruber Syndrome is a rare syndrome inherited as Mendelian autosomal recessive condition. The affected infant usually has a large occipital encephalocoele associated with renal cysts and sometimes polydactyly. The prognosis is poor. The affected child is still born or dies early in infancy. If diagnosis is done by prenatal ultrasound examination termination of pregnancy can be done.
    [Abstract] [Full Text] [Related] [New Search]