| Literature DB >> 22935661 |
Jeffrey R Andolina1, Colleen B Morrison, Alexis A Thompson, Sonali Chaudhury, A Kyle Mack, Maria Proytcheva, Seth J Corey.
Abstract
Exocrine pancreatic insufficiency and diarrhea have been hallmarks in the diagnosis of Shwachman-Diamond syndrome (SDS). We report 2 cases of genetically confirmed SDS in patients who presented with an unusual phenotype. Patient #1 presented with pancytopenia without other system involvement, while patient #2 presented with severe neutropenia, anemia, and a bifid thumb. Neither patient had diarrhea or malabsorption. Both patients had the classic heterozygous mutations c183_184 TA>CT and c.258+2 T>C in the Shwachman-Bodian-Diamond syndrome gene. Incomplete phenotypes may be more common than previously recognized in bone marrow failure syndromes; gastrointestinal symptoms should not be considered a prerequisite for SDS.Entities:
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Year: 2013 PMID: 22935661 PMCID: PMC3514592 DOI: 10.1097/MPH.0b013e3182667c13
Source DB: PubMed Journal: J Pediatr Hematol Oncol ISSN: 1077-4114 Impact factor: 1.289