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Rothmund-Thomson syndrome type 1

rare

Rothmund-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.

Causal genes
ANAPC1
Also known as
poikiloderma of Rothmund-Thomson type 1 · Rothmund-Thomson syndrome, type 1 · RTS1

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