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'Disease Mcardle'
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Disease Mcardle
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Topics Related to Disease Mcardle
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Inborn errors of metabolism
(8)
McArdle disease
Cori disease
GSD type II
Von Gierke disease
Glycogen storage disease
Glycogen storage disease
Leukodystrophy, globoid cell
Galactosemias
Inborn error of metabolism
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Autosomal recessive disorders
Phosphofructokinase deficiency
Multiple sulfatase deficiency
McArdle disease
Cori disease
GSD type II
Von Gierke disease
Leukodystrophy, globoid cell
Genetic disorders
(13)
Amylopectinosis
Hyperostosis, cortical, congenital
Adrenoleuk- odystrophy
Hereditary sensory and autonomic neuropathies
Fukuyama type muscular dystrophy
Fukuyama type muscular dystrophy
McArdle disease
Cori disease
GSD type II
Von Gierke disease
Phosphofructokinase deficiency
Leukodystrophy, globoid cell
Galactosemias
Multiple sulfatase deficiency
more...
Metabolic disorders
Glycogen synthase deficiency
Leukodystrophy, globoid cell
Galactosemias
Hepatology
(8)
Glycogen
Hepatomegaly
Glycogen synthase deficiency
Cori disease
GSD type II
GSD type II
Amylopectinosis
Von Gierke disease
Glycogen storage disease
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Nutrition disorder
Hers' Disease
Glycogen synthase deficiency
Amylopectinosis
Symptoms
Exercise intolerance
Muscle weakness
Muscle pain
Mental retardation
Diseases and disorders
(37)
Glossopharyngeal nerve diseases
Type i complex regional pain syndrome
Myopathies, structural, congenital
Enterocolitis, pseudomembranous
Physiologic nystagmus
Physiologic nystagmus
Histiocytosis non-langerhans-cell
Postpoliomyelitis syndrome
Encephalitis, arbovirus
Olfaction disorders
Intervertebral disk displacement
Rosenthal syndrome
Morvan disease
Metatropic dwarfism
Myoglobinuria
Brachial plexus neuropathies
Optic neuropathy, ischemic
Marinesco sjogren syndrome
Myotubular myopathy
Meniscus tear
GSD type II
Amylopectinosis
Phosphofructokinase deficiency
Hyperostosis, cortical, congenital
Purpura, schoenlein-henoch
Glycogen storage disease
Hereditary sensory and autonomic neuropathies
Leukodystrophy, globoid cell
Fetofetal transfusion
Lupus erythematosus, cutaneous
Polyendocr- inopathies, autoimmune
Fukuyama type muscular dystrophy
Galactosemias
Multiple sulfatase deficiency
Inborn error of metabolism
Rhabdomyolysis
Myelodysplastic syndromes
Mental retardation
more...
Signs and tests
Electromyography (EMG)
Lactic acid in blood
Magnetic resonance imaging
Myoglobin in urine
Serum creatine kinase
See also
(18)
Purpura, schoenlein-henoch
Fetofetal transfusion
Lupus erythematosus, cutaneous
Polyendocr- inopathies, autoimmune
Phosphorylase
Phosphorylase
Dominance (genetics)
Lysosomal storage disease
Lysosome
Renal failure
Www.agsdus.org
Dysplasia
Creatine kinase
Muscle biopsy
Rhabdomyolysis
Mycosis fungoides
Myelodysplastic syndromes
Emedicine
Glycogen phosphorylase
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