|
|
We experienced two cases of Werdnig-Hoffmann Disease in a 23 minths old boy & 15 months old
boy with the complaint of progressive muscular weakness on both extremities. There development
has been almost normal until 3 month of life in case 1 and until 8 month of life in case 2. Diagnosis
was based on clinical features, electromyography and muscle biopsy. We report... |
