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 …

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 …

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 …

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 …

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

Werner syndrome is an adult-onset progeria syndrome that results in various complications.
This study aimed to clarify the profile and secular variation of the disease. Fifty-one patients …

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

Progeria syndromes are rare disorders that involve premature aging. Mutations in BANF1
have been recently reported to cause a new hereditary progeroid syndrome that we now …