Infant Boy with Microcephaly Gastroesophageal Reflux and Nephrotic Syndrome (Galloway-Mowat Syndrome): A Case Report
Abstract
In this case report, we present the first diagnosed case of Galloway- Mowat syndrome in Iran. A 7 month old infant boy with microcephaly that had prominently stunted head growth after birth, gastroesophageal reflux, multiple craniofascial characters, hypothyroidism and nephrotic syndrome diagnosed at 5 months of age associated with rapid decline in renal function and heavy proteinuria in 2 months .
Keywords
Microcephaly;Nephrotic syndrome; Esophageal reflux; Galloway- Mowat syndrome
Full Text:
PDFDOI: http://dx.doi.org/10.15171/middle%20east%20j%20di.v4i1.681
This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.