Affiliation:
1. Charing Cross Hospital Medical School, University of London, England.
Abstract
Abstract
The occurrence of congenital hypoplastic thrombocytopenia with absent radii is described in siblings.
Both presented with hemorrhagic manifestations within a few weeks of birth and the first died at the age of six and a half months.
Reference is made to two other examples in siblings.
These abnormalities are considered as due to a genetic defect and the cases are probably variants of Fanconi’s syndrome.
Publisher
American Society of Hematology
Subject
Cell Biology,Hematology,Immunology,Biochemistry
Cited by
59 articles.
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