Severe congenital Factor VII deficiency associated with the 13q deletion syndrome

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Abstract

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.

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