| Literature DB >> 17212731 |
Abstract
In an analysis of 804 haemophilia pedigrees, mild to moderate haemophilia A or B was found to be clearly familial in 70% of cases, severe haemophilia B in 57% of cases and severe haemophilia A in 45% of cases. The rest of the patients were 'sporadic' i.e., either isolated cases or brothers in the first affected sibship. In sporadic families, 88% of mothers but only 19% of maternal grandmothers had the relevant mutation in their white blood cells. Among patients with familial haemophilia, half the patients with mild haemophilia and those with severe haemophilia B had a direct male ancestor with haemophilia, but only 28% of patients with severe haemophilia A had such a progenitor.Entities:
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Year: 2007 PMID: 17212731 DOI: 10.1111/j.1365-2516.2006.01397.x
Source DB: PubMed Journal: Haemophilia ISSN: 1351-8216 Impact factor: 4.287