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Kugelberg Welander Syndrome


the main title of the report Kugelberg Welander Syndrome is not the name you expected. Please check the synonyms listing to find the alternate name

Important

It is possible that the main title of the report Kugelberg Welander Syndrome is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report.

Synonyms

  • Juvenile Spinal Muscular Atrophy Type III
  • KWS
  • SMA III
  • Spinal Muscular Atrophy Type III

Disorder Subdivisions

None

General Discussion

Kugelberg-Welander Syndrome is a rare inherited disorder. Major symptoms may include wasting and weakness in the muscles of the arms and legs, twitching, clumsiness in walking, and eventual loss of reflexes. Kugelberg- Welander Syndrome is not apparent at birth, it usually appears during the first 10 to 20 years of life.


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