"See also "
"Fukuyama congenital muscular dystrophy"
"Santavuori muscle-eye-brain (MEB) Finnish-type"
Expected headings
"See also "
"There is a wide spectrum of clinical manifestations in the different types of congenital muscular dystrophies, from a severe and often early fatal infant syndrome with feeding and respiratory troubles to a moderate motor delay and mild or moderate limb-girdle involvement during childhood, compatible with survival into adult life 3,5. Common symptoms are:"
"CMD 2, 3 and 4, belong to the group of dystroglycanopathies, which frequently have brain involvement. This group also includes limb-girdle muscular dystrophy which is midler without CNS involvement 10."