𝔖 Bobbio Scriptorium
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Clinical phenotype in congenital muscular dystrophy: correlation with expression of merosin in skeletal

✍ Scribed by J. Philpot; C. Sewry; J. Pennock; V. Dubowitz

Book ID
116168520
Publisher
Elsevier Science
Year
1995
Tongue
English
Weight
361 KB
Volume
5
Category
Article
ISSN
0960-8966

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In typical Fukuyama congenital muscular dystrophy (FCMD), peak motor function is usually only unassisted sitting or sliding on the buttocks, though a few patients are able to walk at some point. However, a few patients have a severe phenotype and never acquire head control. In addition, it is clinic