Werner syndrome

A rare inherited syndrome characterized by premature aging with onset in the third decade of life and with cardinal clinical features including bilateral cataracts, short stature, graying and thinning of scalp hair, characteristic skin disorders and premature onset of additional age-related disorders.

Also known as: WS, Werner syndrome, Werner's syndrome, adult premature aging syndrome, adult progeria, WRN

2 clinical trials for this condition and its sub-types.