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  • Title: Galloway-Mowat syndrome.
    Author: Akhtar N, Kiran S, Hafeez F.
    Journal: J Coll Physicians Surg Pak; 2008 Aug; 18(8):520-1. PubMed ID: 18798594.
    Abstract:
    Galloway-Mowat syndrome is a rare multisystem genetic disorder with constellation of neurological, skeletal, growth, facial, gastrointestinal and renal abnormalities. This case report describes Galloway-Mowat syndrome in a young boy suffering from congenital microcephaly, developmental delay, seizures and various dysmorphic features in whom nephrotic syndrome became apparent at 5 years of age.
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