WT limb-blood syndrome

WT limb-blood syndrome is characterized by hematological anomalies (Fanconi anemia, leukemia and lymphoma) often appearing during childhood. Anomalies of the limbs and hands are also present: bifid or hypoplastic thumbs, cutaneous syndactyly, and ulnar and radial defects. The syndrome has been described in several families. Transmission is autosomal dominant.

Also known as: WT limb-blood syndrome, WT limb blood syndrome, WTsyndrome, radial-ulnar hypoplasia with bone marrow failure and/or leukaemia, radial-ulnar hypoplasia with bone marrow failure and/or leukemia

9 clinical trials for this condition and its sub-types, 0 tagged with WT limb-blood syndrome itself.