Abstract
Summary A new syndrome of congenital hypoplastic anemia and triphalangeal thumbs has been found in two brothers, at least one of whom also has a congenital heart defect. It is not possible from the present data to discriminate between X-linked and autosomal recessive modes of inheritance. This condition is clearly distinguishable from Fanconi's fancytopenia, the radial aplasia-thrombocytopenia, and the Holt-Oram syndromes by physical and hematologic criteria.
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