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Severe congenital Factor VII deficiency associated with the 13q deletion syndrome
Author(s) -
Hewson Michael P.,
Carter John M.
Publication year - 2002
Publication title -
american journal of hematology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.456
H-Index - 105
eISSN - 1096-8652
pISSN - 0361-8609
DOI - 10.1002/ajh.10237
Subject(s) - disease , medicine , pediatrics
The first reported case of clinically significant congenital Factor VII deficiency in association with the 13q deletion syndrome is presented. It illustrates the importance of knowledge of the specific genes involved in gross deletion syndromes and adds to the current clinical experience of this rare disease. Am. J. Hematol. 71:232–233, 2002. © 2002 Wiley‐Liss, Inc.