Werner syndrome (WS), also known as adult progeria, is a premature ageing syndrome that
can manifest itself with grey hair, hair loss, diabetes mellitus, hyperlipidaemia, hypertension …

Werner syndrome (WS) is an autosomal recessive disorder characterised by premature
ageing. WS patients often experience scleroderma-like manifestation including skin …

Werner's syndrome (WS) is an autosomal recessive disorder characterized by premature
aging. The main features of the disease are scleroderma-like skin appearance, premature …

A59-year-old woman had been under follow-up since child-hood because of juvenile
scleroderma and recurrent calcinosis. Her symptoms began gradually at age 15 years with …

We report two cases of Werner's syndrome (WS). First, a 42-year-old Japanese man was
referred on suspicion of systemic sclerosis (SSc) because of scleroderma-like skin atrophy …

A síndrome de Werner é uma doença autossômica recessiva rara associada a
envelhecimento precoce, cujo quadro cutâneo deve ser distinguido daquele encontrado na …

Werner syndrome (WS) is rare adult-onset progeria characterized by premature aging and
early death. Patients develop normally until adolescence and usually present in early …

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 …

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 …

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