J Korean Pediatr Soc.  1978 Aug;21(8):623-629.

A Case of Aeute Werdnig-Hoffmann Disease

Affiliations
  • 1Department of Pediatrics, Seoul Red Cross Hospital, Korea.
  • 2Department of Pathology, College of Medicine, Seoul National University, Korea.

Abstract

Acute Werdnig-Hoffmann disease is genetically determined progressive degenerative disease of anterior spinal neuron, characterized by fasciculations of the tongue usually occuring along with flaccid paralysis of extremities with intact mentality. We experienced a 5 months old female infant, whose sister died of pneumonia at the age of 2 months, had same symptoms and signs : revealing hypotonic state with flaccid extremities only responding to painful stimuli, and paradox-ical respiration. She was alert in mental state and showing typical tongue fasciculation even in quiet state. Muscle biopsy finding was compatible with acute werdnig-Hoffmann disease and serum enzymes were normal value.


MeSH Terms

Biopsy
Extremities
Fasciculation
Female
Humans
Infant
Neurons
Paralysis
Pneumonia
Reference Values
Respiration
Siblings
Spinal Muscular Atrophies of Childhood*
Tongue
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