Werner syndrome (WS) is a rare autosomal recessive adult-onset progeroid disorder
characterized by the early onset of aged-appearance and age-related metabolic disorders …

Introduction: Werner's Syndrome (WS) is a rare autosomal recessive adult onset progeroid
disorder characterized by the early onset of aged-appearance and age related metabolic …

Werner syndrome is a rare autosomal recessive premature progeroid syndrome caused by
mutations in the WRN gene. It is characterized by early onset of age‐related diseases, such …

Background. Progeroid syndromes are a group of rare hereditary diseases characterized by
accelerated aging of the body. The most striking signs of premature aging are manifested in …

Werner syndrome, also called adult progeria, is a heritable autosomal recessive human
disorder characterized by the premature onset of numerous age-related diseases including …

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 …

Introduction Le syndrome de Werner (SW) est une maladie génétique rare caractérisée par
un vieillissement cutané précoce et des manifestations systémiques diverses. Les …

Background: Werner syndrome (WS; MIM# 277700) is a rare genetic disorder characterized
by accelerated aging and predisposition to cancers. The causal gene, WRN, encodes a …

We report the clinical course of two siblings with Werner′ s syndrome (WS) who were
diagnosed and followed at our clinics for 12 years. Initial diagnosis of the first sibling (sister) …