METHODS An English language literature search of WS was performed. Based on the
availability and completeness of clinical descriptions, 24 references containing a total of 66 …

IN 1904, Otto Werner (1) described a syndrome called “cataract in connection with
scleroderma" which involved 2 brothers and 2 sisters in a family of 6 children. Thirty years …

Werner’s syndrome may be lost in the shadow of the scleroderma | SpringerLink Skip to main
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Werner's syndrome is a rare condition usually presenting as premature ageing in adults.
Over a period of 30 years we have followed two siblings with extensive musculoskeletal …

The case of a 40-year-old woman with Werner's syndrome associated with systemic lupus
erythematosus (SLE) is reported. The patient exhibited short stature, slender extremities …

Twenty‐four cases of Werner's syndrome were studied to define the clinical manifestations
in comparison with those found in a clinical review of 153 cases in the Japanese medical …

Werner syndrome is an autosomal-recessive disease characterized by premature aging,
shortness of stature, scleroderma-like skin changes, endocrine abnormalities, and cataracts …

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 …

The autopsy findings in a 29‐year‐old male with Werner's syndrome are presented, with a
review of similar data on 17 autopsy cases reported in the literature. The pathologic findings …

Werner's syndrome is believed to be an autosomal‐recessive inherited disorder. Among
other manifestations of premature aging, patients with Werner's syndrome frequently …