Werner syndrome (WS) is an autosomal recessive syndrome characterized by genomic
instability that affects multiple body systems. The characteristic features of the disease …

Werner syndrome is a rare autosomal recessive disorder, caused by mutations in the WRN
gene. Clinical findings include: senile appearance, short stature, grey hair, alopecia, bird …

Werner's syndrome (WS) is an autosomal recessive genetic disease, which is mainly
characterized by scleroderma-like skin changes, juvenile cataracts, short stature, and signs …

Werner's syndrome (WS) is an autosomal recessive genetic disease, which is mainly
characterized by scleroderma‐like skin changes, juvenile cataracts, short stature, and signs …

INTRODUCTION: Werner's syndrome, a rare autosomal recessive genetic disease, is a
premature aging disease characterized by early onset of symptoms related to normal aging …

Background: Werner syndrome is a rare autosomal recessive disease caused by a mutation
of the DNA helicase gene (WRN), characterized by the premature onset of multiple age …

Werner syndrome (WS) is an autosomal recessive progeroid disorder caused by mutations
in the WRN DNA helicase. It is characterized by the graying and loss of hair, juvenile …

Werner syndrome is a rare, autosomal recessive condition with multiple progeroid features,
but it is a phenocopy of aging rather than accelerated or premature senescence. Somatic …

Patients with Werner's syndrome almost invariably have disorders of the skin or its
appendages; therefore, dermatologists should be aware of the typical clinical picture …

Werner's syndrome is a rare inherited disorder characterized by short stature, sclerosed
skin, cataract and premature aging of the face. The disease involves multiple systems of the …