| Literature DB >> 25154619 |
Elpis Mantadakis1, Julie Sawalle-Belohradsky, Marianna Tzanoudaki, Maria Kanariou, Athanassios Chatzimichael, Michael H Albert.
Abstract
The authors describe two young brothers and a 12-year-old male with long-standing thrombocytopenia with normal sized platelets, in whom novel mutations of the WAS gene were identified. Their clinical picture and the in vitro assessment of the T-cell function were consistent with X-linked thrombocytopenia (XLT). A high index of suspicion for XLT is required, even in the setting of normal sized platelets for males with affected maternally-related male family members, and males with moderately severe chronic thrombocytopenia that have failed to respond to treatments that are usually effective for immune thrombocytopenia.Entities:
Keywords: WAS gene; Wiskott-Aldrich syndrome; X-linked thrombocytopenia; mutations
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Year: 2014 PMID: 25154619 DOI: 10.1002/pbc.25196
Source DB: PubMed Journal: Pediatr Blood Cancer ISSN: 1545-5009 Impact factor: 3.167