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Rothmund-Thomson syndrome type 1
rareRothmund-Thomson syndrome type 1 is a subform of Rothmund-Thomson syndrome (RTS) presenting with a characteristic facial rash (poikiloderma) and frequently associated with short stature, sparse scalp hair, sparse or absent eyelashes and/or eyebrows, and rapidly progressive bilateral juvenile cataracts. In contrast to RTS2, patients with RTS1 do not appear to have an increased risk of developing cancer.
- Identifiers
- MONDO:0016368 OMIM:618625Orphanet:221008
- Causal genes
- ANAPC1
- Part of
- Rothmund-Thomson syndrome
- Also known as
- poikiloderma of Rothmund-Thomson type 1 · Rothmund-Thomson syndrome, type 1 · RTS1
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