Serial MRI in Fukuyama type congenital muscular dystrophy
โ Scribed by M. Aihara; Y. Tanabe; K. Kato
- Publisher
- Springer
- Year
- 1992
- Tongue
- English
- Weight
- 870 KB
- Volume
- 34
- Category
- Article
- ISSN
- 0028-3940
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๐ SIMILAR VOLUMES
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
Fukuyama type congenital muscular dystrophy (FCMD) is an autosomal recessive disorder characterized by a combination of primary muscular dystrophy of early infantile onset and brain malformation (lissencephaly type 11). The identification of the FCMD gene locus at 9q31 opened the theoretical possibi