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Galloway-Mowat syndrome
JCPSP-Journal of the College of Physicians and Surgeons Pakistan. 2008; 18 (8): 520-521
in English | IMEMR | ID: emr-102933
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 nephritic syndrome became apparent at 5 years of age
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Index: IMEMR (Eastern Mediterranean) Main subject: Seizures / Abnormalities, Multiple / Fetal Growth Retardation / Genetic Diseases, Inborn / Hernia, Hiatal / Microcephaly / Nephrotic Syndrome Type of study: Case report Limits: Female / Humans / Male Language: English Journal: J. Coll. Physicians Surg. Pak. Year: 2008

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Index: IMEMR (Eastern Mediterranean) Main subject: Seizures / Abnormalities, Multiple / Fetal Growth Retardation / Genetic Diseases, Inborn / Hernia, Hiatal / Microcephaly / Nephrotic Syndrome Type of study: Case report Limits: Female / Humans / Male Language: English Journal: J. Coll. Physicians Surg. Pak. Year: 2008