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WT limb-blood syndrome
rareWT 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.
- Identifiers
- MONDO:0008688 OMIM:194350Orphanet:3466
- Part of
- Inherited aplastic anemia
- Also known as
- radial-ulnar hypoplasia with bone marrow failure and/or leukaemia · radial-ulnar hypoplasia with bone marrow failure and/or leukemia · WT limb blood syndrome · WTsyndrome
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