Other terms
Rothmund Thomson Syndrome,Syndrome, Rothmund-Thomson,Poikiloderma of Rothmund-Thomson,Poikiloderma of Rothmund Thomson,Rothmund-Thomson Poikiloderma,Rothmund-Thomson Poikilodermas,Poikiloderma Atrophicans and Cataract,Poikiloderma Congenitale,Congenitale, Poikiloderma,Congenitales, Poikiloderma,Poikiloderma Congenitales
Description
Rothmund-Thomson Syndrome: An autosomal recessive syndrome occurring principally in females, characterized by the presence of reticulated, atrophic, hyperpigmented, telangiectatic cutaneous plaques, often accompanied by juvenile cataracts, saddle nose, congenital bone defects, disturbances in the growth of HAIR; NAILS; and TEETH; and HYPOGONADISM.
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