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Metabolic Myopathy
Metabolic myopathy
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Muscular disorders
(22)
Central core disease
Centronuclear myopathy
Congenital myopathies
Inclusion body myositis
Mitochondrial myopathy
Mitochondrial myopathy
Myopathy
Nemaline myopathy
Polymyositis
Arthrogryposis
Chronic progressive external ophthalmoplegia
Diastasis recti
Laminopathy
Macrophagic myofasciitis
Muscular dystrophy
Myokmia
Orofacial myological disorders
Pelvic Floor Muscle Disorder
Thyrotoxic myopathy
Torticollis
Writer's cramp
X-linked myotubular myopathy
Zenker's degeneration
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Inborn errors of metabolism
(9)
SCAD deficiency
Carnitine palmitoylt- ransferase deficiency
Carnitine palmitoylt- ransferase II deficiency
Myoadenylate deaminase deficiency
Metabolic diseases
Metabolic diseases
McArdle disease
Acid maltase deficiency
Glycogenosis
Carnitine deficiency
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Autosomal recessive disorders
(8)
Multiple sulfatase deficiency
SCAD deficiency
Carnitine palmitoylt- ransferase deficiency
Carnitine palmitoylt- ransferase II deficiency
McArdle disease
McArdle disease
Nemaline myopathy
Acid maltase deficiency
Carnitine deficiency
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Genetic disorder
Fukuyama type muscular dystrophy
Ragged red fibers
SCAD deficiency
Congenital myopathies
Mitochondrial diseases
(16)
Mitochondrial encephalomyopathies
Myopathy, Mitochondr- ial-Encephalopathy-Lactic Acidosis-Stroke
Diabetes mellitus and deafness
Friedreich's ataxia
Kearns-Sayre syndrome
Kearns-Sayre syndrome
Leber's hereditary optic neuropathy
Leigh's disease
Mitochondrial myopathy
Myoneurogenic gastrointestinal encephalopathy
Neuropathy, ataxia, and retinitis pigmentosa
Nonsyndromic deafness
Pearson syndrome
Progressive external ophthalmoplegia
Ragged red fibers
Threshold expression
Wolfram syndrome
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Muscular dystrophy
Dystrophin
Myotonic dystrophy
Fukuyama type muscular dystrophy
Rare diseases
Endocardial fibroelastosis
Myositis ossificans
Malignant hyperthermia
Carnitine palmitoylt- ransferase deficiency
Multiple sulfatase deficiency
Acid maltase deficiency
Neurology
Muscle weakness
Lgmd
Movement disorders
Myasthenia gravis
Neuropathy
Mitochondrial encephalomyopathies
Myotonic dystrophy
Disorders of muscles
(8)
Myositis
Strain (injury)
Compartment syndrome
Contracture
Fibrodysplasia ossificans progressiva
Fibrodysplasia ossificans progressiva
Muscle atrophy
Myositis ossificans
Pyomyositis
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Neurological disorders
Paramyotonia congenita
Chronic fatigue syndrome
Central core disease
Nemaline myopathy
Neuropathy
Muscular system
Myalgia
Muscle biopsy
Skeletal muscles
Neuromuscular diseases
Dystrophin
Acid-base disturbances
(14)
Metabolic acidosis
Metabolic alkalosis
Respiratory acidosis
Acid-base homeostasis
Acid-base imbalance
Acid-base imbalance
Acidosis
Alkalosis
Anion gap
Hyperchloremic acidosis
Ketoacidosis
Lactic acidosis
Renal compensation
Respiratory alkalosis
Respiratory compensation
more...
Symptoms
Exercise intolerance
Hypotonia
Mental retardation
Myalgia
Muscle weakness
Movement disorders
Diseases and disorders
(54)
Barcoo Fever
Lipid storage myopathy
Mitochondrial myopathy-e- ncephalopathy-lactic acidosis
Dermatomyositis
Morvan disease
Morvan disease
Rhabdomyolysis
Lactate dehydrogenase deficiency
Metatropic dwarfism
Phosphoglycerate kinase deficiency
Fatty acid oxidation disorders
Inflammatory myopathy
Myoglobinuria
Meniscus tear
Eosinophilia myalgia syndrome
Cardiomyopathy
Neutropenia
Hypokalemic
Metabolic disorders
Aplasia
Myopathy
Myopathy, Mitochondr- ial-Encephalopathy-Lactic Acidosis-Stroke
3-Methylglutaconic aciduria type II
Mitochondrial myopathy
Fukuyama type muscular dystrophy
Carnitine palmitoylt- ransferase II deficiency
Congenital myopathies
Myositis
Multiple sulfatase deficiency
Centronuclear myopathy
Myoadenylate deaminase deficiency
Central core disease
Marinesco sjogren syndrome
Metabolic diseases
Nemaline myopathy
Endocardial fibroelastosis
Acid maltase deficiency
Myositis ossificans
Hypotonia
Lgmd
Periodic paralysis
Glycogenosis
Bethlem myopathy
Polymyositis
Movement disorders
Metabolic alkalosis
Paramyotonia congenita
Carnitine deficiency
Myasthenia gravis
Myotonic dystrophy
Strain (injury)
Mental retardation
Malignant hyperthermia
Neuropathy
Chronic fatigue syndrome
more...
See also
(20)
John Clark, Jr.
3-Methylglutaconic aciduria type II
Cytochrome-c oxidase deficiency
Myophosphorylase
Withdrawal syndromes
Withdrawal syndromes
Marinesco sjogren syndrome
HMG-CoA reductase inhibitors
Statins
Humberto Cota
Mullerian duct
X linked
Myoneural junction
Autosomal recessive
Glycogen
Periodic paralysis
Bethlem myopathy
Pavlos Melas
Respiratory chain
Performance enhancing drugs
Acyl CoA dehydrogenase
more...
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