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Permanent muscle weakness in McArdle disease.
- Source :
-
Muscle & nerve [Muscle Nerve] 2009 Sep; Vol. 40 (3), pp. 350-7. - Publication Year :
- 2009
-
Abstract
- McArdle disease is an autosomal recessive muscle glycogenosis. In the typical clinical presentation, only exercise-related symptoms are noted. Nevertheless, permanent weakness may occur, usually late in life. In this study we report on the clinical and genetic features of fixed muscle weakness in McArdle disease. Among the 80 McArdle patients being followed at the Institute of Myology of the Salpêtrière Hospital, 9 patients have permanent weakness. The diagnosis of McArdle disease was confirmed by muscle biopsy and genetic investigations. Two patterns of muscle weakness and wasting were noted: (1) proximal and symmetric in 5 patients; and (2) asymmetric, mimicking facioscapulohumeral dystrophy (FSHD) in 4 patients. Computerized tomography scan showed fatty infiltration in the shoulder and pelvic girdle muscles. There was no clear correlation between genotype and the severity of muscle weakness. Proximal muscle weakness appeared after the age of 40 years and affected 11% of subjects in our series of 80 McArdle patients. Among patients over 40 years of age, 37.5% had muscle weakness.
- Subjects :
- Aged
Cohort Studies
DNA Mutational Analysis
Electromyography methods
Female
Genetic Predisposition to Disease
Glycogen Phosphorylase, Muscle Form genetics
Glycogen Storage Disease Type V genetics
Humans
Male
Middle Aged
Muscle Weakness genetics
Muscle Weakness pathology
Muscle, Skeletal pathology
Muscular Dystrophy, Facioscapulohumeral diagnosis
Mutation genetics
Myoglobinuria etiology
Myoglobinuria genetics
Tomography Scanners, X-Ray Computed
Glycogen Storage Disease Type V complications
Glycogen Storage Disease Type V pathology
Muscle Weakness etiology
Subjects
Details
- Language :
- English
- ISSN :
- 0148-639X
- Volume :
- 40
- Issue :
- 3
- Database :
- MEDLINE
- Journal :
- Muscle & nerve
- Publication Type :
- Academic Journal
- Accession number :
- 19670320
- Full Text :
- https://doi.org/10.1002/mus.21351