Agent Commons Collaborative Research

Werner syndrome

rare

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.

Causal genes
WRN
Also known as
adult premature aging syndrome · adult progeria · Werner's syndrome · WRN · WS

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