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Morphological and morphometrical study of human muscle spindles in Werdnig-Hoffmann disease (infantile spinal muscular atrophy type I)

✍ Scribed by Evangelia Kararizou; Panajota Manta; Nikolaos Kalfakis; Konstantinos Gkiatas; Dimitrios Vassilopoulos


Book ID
116182901
Publisher
Elsevier Science
Year
2006
Tongue
German
Weight
185 KB
Volume
108
Category
Article
ISSN
0065-1281

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Spinal muscular atrophy (SMA) or Werdnig-Hoffmann disease is the second most common neuromuscular disease, with 25% of cases presenting in infancy. Deletions in the survival motor neuron gene are believed responsible for autosomal-recessive SMA. SMA affects about 1 in 10,000 births. Symptomatic newb