Infant Boy with Microcephaly Gastroesophageal Reflux and Nephrotic Syndrome (Galloway-Mowat Syndrome): A Case Report
نویسندگان
چکیده
In this case report, we present the first diagnosed case of Galloway-Mowat syndrome in Iran. A 7 month old infant boy withmicrocephaly that had prominently stunted head growth afterbirth, gastroesophageal reflux, multiple craniofascial characters,hypothyroidism and nephrotic syndrome diagnosed at 5 monthsof age associated with rapid decline in renal function and heavyproteinuria in 2 months .
منابع مشابه
Galloway-Mowat syndrome.
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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عنوان ژورنال:
دوره 4 شماره
صفحات -
تاریخ انتشار 2012