Werner syndrome (WS), also known as adult progeria, is a rare autosomal recessive
inherited progeroid syndrome characterised by multiple features consistent with accelerated …

Abstract Werner syndrome (WS; MIM# 277700) or adult progeria, is a rare disease,
associated with mutations of a single gene (RECQL2 or WRN), located on chromosome 8 …

Werner's syndrome (WS) or progeria adultorum is a heritable autosomal recessive disease
in which the aging process is accelerated, just after puberty. It is caused by mutations in the …

Werner syndrome (ie, adult progeria) is a rare autosomal recessive disorder caused by
mutations of the WRN gene, which is characterized by the premature appearance of features …

A 33-year-old female was referred with osteoporosis. She was seen as a child by
paediatricians for failure to thrive. She suffered from irregular periods throughout puberty …

Progeria is a premature ageing syndrome. Werner Syndrome (WS) is a type of progeria in
the adult which includes bilateral juvenile cataracts and cutaneous sclerodermiform …

Werner's syndrome (adult onset progeria) is a rare form of autosomal recessive
genodermatosis associated in almost 80% of cases with mutation of the WRN gene. This …

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

Progeroid syndromes (PSs) constitute a group of disorders characterized by clinical features
mimicking physiological aging at an early age. In some of these syndromes, biological …

Segmental progeroid syndromes are a group of disorders with multiple features resembling
accelerated aging. Adult-onset Werner syndrome (WS) and childhood-onset Hutchinson …