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Rothmund-Thomson syndrome type 2
rareRothmund-Thomson syndrome type 2 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, congenital bone defects and an increased risk of osteosarcoma in childhood and squamous cell carcinoma later in life.
- Identifiers
- MONDO:0016369 OMIM:268400Orphanet:221016
- Causal genes
- RECQL4
- Also known as
- poikiloderma of Rothmund-Thomson type 2 · Rothmund-Thomson syndrome, type 2 · RTS2
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