Congenital muscular dystrophy with primary laminin alpha2 (merosin) deficiency presenting as inflammatory myopathy.

Pegoraro, E

Congenital muscular dystrophy with primary laminin alpha2 (merosin) deficiency presenting as inflammatory myopathy. [electronic resource] - Annals of neurology Nov 1996 - 782-91 p. digital

Publication Type: Case Reports; Journal Article; Research Support, U.S. Gov't, P.H.S.

0364-5134

10.1002/ana.410400515 doi


Base Sequence
Biopsy
Child
Child, Preschool
Deoxyribonucleases, Type II Site-Specific
Electromyography
Female
Humans
Infant
Infant, Newborn
Inflammation
Laminin--deficiency
Middle Aged
Motor Activity
Muscle, Skeletal--pathology
Muscular Dystrophies--congenital
Nuclear Family
Pedigree
Point Mutation
Polymerase Chain Reaction
Polymorphism, Restriction Fragment Length
Polymorphism, Single-Stranded Conformational
Polymyositis--physiopathology
Sequence Deletion