Shwachman-Diamond syndrome presenting in a premature infant as pancytopenia

Shwachman–Diamond syndrome is a rare autosomal recessive disorder characterized by bone marrow dysfunction, exocrine pancreatic insufficiency, failure to thrive, and skeletal abnormalities. It is most commonly diagnosed in early childhood after the development of hematologic abnormalities. We report...

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Veröffentlicht in:Pediatric blood & cancer 2008-07, Vol.51 (1), p.123-124
Hauptverfasser: Black, L. Vandy, Soltau, Thomas, Kelly, David R., Berkow, Roger L.
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Sprache:eng
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Zusammenfassung:Shwachman–Diamond syndrome is a rare autosomal recessive disorder characterized by bone marrow dysfunction, exocrine pancreatic insufficiency, failure to thrive, and skeletal abnormalities. It is most commonly diagnosed in early childhood after the development of hematologic abnormalities. We report a premature infant born at 33 weeks gestation who was small for gestational age and displayed persistent cytopenias requiring transfusion. Genetic testing confirmed a diagnosis of Shwachman–Diamond syndrome (SDS). Pediatr Blood Cancer 2008;51:123–124. © 2008 Wiley‐Liss, Inc.
ISSN:1545-5009
1545-5017
DOI:10.1002/pbc.21550