|
|
A case of Werdnig-Hoffmann disease (Kugelberg-Welander type), rare neuromuscular disease in
childhood, was presented in a 11 years old Korean boy.
The patient was well until 3yrs of age, when he was found to have muscle weakness of both upper
and lower extremity. At the time of admission he showed emaciated, and flaccid apperance with
tongue fasciculation.
Diagnosis was established by clinical teature, eletromyography, and... |
