A Case of Shwachman–Diamond Syndrome who Presented with Hypotonia

Author:

Özçay Figen1,Olcay Lale2,Ceylaner Serdar3,Sezer Taner4,Barış Zeren1

Affiliation:

1. Department of Pediatric Gastroenterology, Başkent University Hospital, Beşevler-Çankaya, Ankara, Turkey

2. Department of Pediatric Hematology, Başkent University Hospital, Beşevler-Çankaya, Ankara, Turkey

3. Medical Genetics, İntergen Laboratory, Ankara, Turkey

4. Department of Pediatric Neurology, Başkent University Hospital, Beşevler-Çankaya, Ankara, Turkey

Abstract

AbstractWe present a patient with failure to thrive and severe hypotonia, who was initially suspected of having a neurometabolic disease but later diagnosed as Shwachman–Diamond syndrome (SDS), which was genetically confirmed. SDS is a multisystemic disease, which is characterized by exocrine pancreatic deficiency, bone marrow dysfunction with increased risk for malignant transformation, and skeletal abnormalities. It should be included in differential diagnosis of patients with failure to thrive and unexplained neurodevelopmental delay with neutropenia.

Publisher

Georg Thieme Verlag KG

Subject

Genetics (clinical),Pediatrics, Perinatology and Child Health

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