J Korean Neurol Assoc.  1984 Jun;2(1):65-70.

A Case of Wohlfart-Kugelberg-Welander Syndrome in Korean Sister

Affiliations
  • 1Department of Neurology, College of Medicine, Hanyang University.

Abstract

Wohlfart et al and then Kugelberg and Welander were concerned with patients suffering from proximal limb weakness that resembled muscular dystrophy, but the muscle biopsy and EMG indicated neuronal disease. However, several reports had determined considerable variation according to age of onset, distribution of weakness and rate of progression. Most of familial cases fit an autosomal recessive pattern but dominant and X-linked forms were recorded. The syndrome is recognized by clinical criteria and laboratory abnormalities only that reflect neuronal degeneration. It merges with Werdnig-Hoffmann disease in infant and with amyotrophic lateral sclerosis in adult and with Wohlfart-Kugelberg-Welander syndrome in adolescent. In this report we respresent a case which is probably Wohlfart-Kugelberg-Welander syndrome in Korean sister.


MeSH Terms

Adolescent
Adult
Age of Onset
Amyotrophic Lateral Sclerosis
Biopsy
Extremities
Humans
Infant
Muscular Dystrophies
Neurons
Siblings*
Spinal Muscular Atrophies of Childhood
Full Text Links
  • JKNA
Actions
Cited
CITED
export Copy
Close
Share
  • Twitter
  • Facebook
Similar articles
Copyright © 2024 by Korean Association of Medical Journal Editors. All rights reserved.     E-mail: koreamed@kamje.or.kr