Werner syndrome
This syndrome, also known as adult progeria and cataract-scleroderma-progeria syndrome, is a congenital autosomal recessive genetic disease characterized by elderly facies, short stature, gray hair in adolescence, juvenile cataracts, scleroderma-like skin changes on the limbs, osteoporosis, tissue calcification, diabetes and gonadal dysgenesis.
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Site of disease:
whole body -
Infectious :
Not contagious -
Frequent population:
Children (mostly children of blood-related marriages)... -
Related symptoms:
Skin atrophy congestion atherosclerosis skin aging abnormal body shape -
Concurrent disease:
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