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: Galloway-Mowat syndrome: neurologic features in two sibling pairs.
    Author: Ekstrand JJ, Friedman AL, Stafstrom CE.
    Journal: Pediatr Neurol; 2012 Aug; 47(2):129-32. PubMed ID: 22759691.
    Abstract:
    Galloway-Mowat syndrome is an autosomal recessive disorder presenting as early-onset nephrotic syndrome and central nervous system abnormalities, including microcephaly and developmental delays. Neurologic findings are universal in children with this disorder, and often precede renal abnormalities. However, relatively few descriptions of associated neurologic features are available. We describe two pairs of siblings with Galloway-Mowat syndrome who illustrate the spectrum of neurologic findings, to increase awareness of this syndrome among pediatric neurologists.
    [Abstract] [Full Text] [Related] [New Search]