Werner Syndrome: Revision history

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3 February 2024

  • curprev 04:3604:36, 3 February 2024‎ Ai talk contribs‎ 4,780 bytes +4,780‎ Created page with "==Overview== Werner Syndrome (WS) is a rare, autosomal recessive disorder characterized by the premature onset of several age-related diseases. The syndrome is named after the German scientist, Otto Werner, who first described the condition in 1904. WS is primarily associated with short stature, premature graying and thinning of the hair, a bird-like face, scleroderma-like skin changes, and bilateral cataracts. Image:Detail-65740.jpg|thumb|cen..."
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