Rothmund-Thomson syndrome

Rothmund-Thomson syndrome (RTS) is a genodermatosis presenting with a characteristic facial rash (poikiloderma) associated with short stature due to pre- and postnatal growth delay, sparse scalp hair, sparse or absent eyelashes and/or eyebrows, juvenile cataracts, skeletal abnormalities, radial ray defects, premature aging and a predisposition to certain cancers.

Also known as: RTS, Rothmund-Thomson syndrome, poikiloderma of Rothmund-Thomson, poikiloderma atrophicans and cataract, poikiloderma congenitale

32 clinical trials for this condition and its sub-types, 1 tagged with Rothmund-Thomson syndrome itself.