myophosphorylase


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my·o·phos·phor·y·lase

(mī'ō-fos-fōr'i-lās),
Muscle phosphorylase
References in periodicals archive ?
Molecular genetic heterogeneity of myophosphorylase deficiency (McArdle's disease).
Histochemical stains showed normal myophosphorylase, phosphofructokinase and myoadenylate deaminase, succinate dehydrogenase, nicotinamide adenine dinucleotide + hydrogen and cytochrome oxidase activity.
The most commonly identified predisposing conditions of ER are deficiencies of carnitine palmitoyltransferase II (CPT2 gene, OMIM *600650), myophosphorylase (McArdle disease, PYGM gene, OMIM *608455), and myoadenylate deaminase (AMPD1 gene, OMIM +102770).
(80,81) In some patients, such persistent symptoms may be related to previously unrecognized neuromuscular disorders, including inflammatory myopathies (81-83); hypothyroidism (84); metabolic myopathies (myophosphorylase deficiency, acid maltase deficiency, and mitochondrial myopathy) (80,85,86); myotonic dystrophy (85); spinal muscular atrophy85; or susceptibility to malignant hyperthermia.
(1984) Muscle fatigue in myophosphorylase deficiency: power spectral analysis of the electromyogram.
Also called: Myophosphorylase deficiency, McArdle's disease, glycogenosis type 5
17D Fort Lee, NJ 07024 (201) 585-0770 http://www.myoclonus.com MYODENYLATE DEAMINASE DEFICIENCY See: Muscular Dystrophy MYOPATHIES, CONGENITAL See: Myotubular Myopathy, X-Linked MYOPATHY, CENTRONUCLEAR See: Myotubular Myopathy, X-Linked; Muscular Dystrophy MYOPATHY, HYPERTHYROID See: Muscular Dystrophy; Thyroid Disorders MYOPHOSPHORYLASE DEFICIENCY See: Glycogen Storage Diseases MYOSITIS See also: Autoimmune Disorders National Myositis Association 7720B El Camino Real, Ste.
Kettering, OH 45409 (513) 293-0409 ??editormdp@aol.com http://www.acor.org/diseases/he matology/mpd 2 MYODENYLATE DEAMINASE DEFICIENCY See: Muscular Dystrophy MYOPATHIES, CONGENITAL See: Myotubular Myopathy, X-Linked MYOPATHY, CENTRONUCLEAR See: Myotubular Myopathy, X-Linked; Muscular Dystrophy MYOPATHY, HYPERTHYROID See: Muscular Dystrophy; Thyroid Disorders MYOPHOSPHORYLASE DEFICIENCY See: Glycogen Storage Diseases MYOSITIS See also: Autoimmune Disorders National Myositis Association 7720B El Camino Real, Ste.
Kettering, OH 45409 (513) 293-0409 ??editormdp@aol.com http://www.acor.org/diseases/hemat ology/mpd 2 MYODENYLATE DEAMINASE DEFICIENCY See: Muscular Dystrophy MYOPATHIES, CONGENITAL See: Myotubular Myopathy, X-Linked MYOPATHY, CENTRONUCLEAR See: Myotubular Myopathy, X-Linked; Muscular Dystrophy MYOPATHY, HYPERTHYROID See: Muscular Dystrophy; Thyroid Disorders MYOPATHY, HYPOTHYROID See: Muscular Dystrophy; Thyroid Disorders MYOPHOSPHORYLASE DEFICIENCY See: Glycogen Storage Diseases MYOSITIS See also: Autoimmune Disorders National Myositis Association 7720B El Camino Real, Ste.