مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

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Information Journal Paper

Title

INFANT BOY WITH MICROCEPHALY GASTROESOPHAGEAL REFLUX AND NEPHROTIC SYNDROME (GALLOWAY-MOWAT SYNDROME): A CASE REPORT

Pages

  52-55

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.

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  • Cite

    APA: Copy

    MALAKI, MAJID, & RAFEEY, MANDANA. (2012). INFANT BOY WITH MICROCEPHALY GASTROESOPHAGEAL REFLUX AND NEPHROTIC SYNDROME (GALLOWAY-MOWAT SYNDROME): A CASE REPORT. MIDDLE EAST JOURNAL OF DIGESTIVE DISEASES (MEJDD), 4(1), 52-55. SID. https://sid.ir/paper/319080/en

    Vancouver: Copy

    MALAKI MAJID, RAFEEY MANDANA. INFANT BOY WITH MICROCEPHALY GASTROESOPHAGEAL REFLUX AND NEPHROTIC SYNDROME (GALLOWAY-MOWAT SYNDROME): A CASE REPORT. MIDDLE EAST JOURNAL OF DIGESTIVE DISEASES (MEJDD)[Internet]. 2012;4(1):52-55. Available from: https://sid.ir/paper/319080/en

    IEEE: Copy

    MAJID MALAKI, and MANDANA RAFEEY, “INFANT BOY WITH MICROCEPHALY GASTROESOPHAGEAL REFLUX AND NEPHROTIC SYNDROME (GALLOWAY-MOWAT SYNDROME): A CASE REPORT,” MIDDLE EAST JOURNAL OF DIGESTIVE DISEASES (MEJDD), vol. 4, no. 1, pp. 52–55, 2012, [Online]. Available: https://sid.ir/paper/319080/en

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