What is the cause of myopathy?

Hypothyroidism prednisone creatine rickets hypokalemia Duchenne muscular dystrophy Colchicine Rosuvastatin Zidovudine Chloroquine MERRF Barth syndrome Myotubular myopathy Walker-Warburg syndrome Alpha-mannosidosis Bethlem myopathy glutaric acidemia type 2 Clevudine AIDS ethanol Atorvastatin simvastatin pravastatin Fanconi syndrome Becker's muscular dystrophy Limb-girdle muscular dystrophy Myoadenylate deaminase deficiency Bezafibrate nemaline myopathy Glycogen storage disease type III Distal muscular dystrophy Telbivudine hereditary inclusion body myopathy Adducted thumb syndrome Myoneurogenic gastrointestinal encephalopathy Fukuyama congenital muscular dystrophy mitochondrial trifunctional protein deficiency Triosephosphate isomerase deficiency Ullrich congenital muscular dystrophy Marinesco-Sjogren syndrome Chanarin-Dorfman disease Glycerol kinase deficiency Emery-Dreifuss muscular dystrophy type 2 Tel Hashomer camptodactyly syndrome Rigid spine muscular dystrophy type 1 Myotubular myopathy, X-linked Carey-Fineman-Ziter syndrome X-linked myopathy with excessive autophagy Calpainopathy Very long-chain acyl-CoA dehydrogenase deficiency Myosin storage myopathy Congenital fiber-type disproportion myopathy Progressive external ophthalmoplegia, autosomal recessive Neutral lipid storage disease with myopathy Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia Lactate dehydrogenase-A deficiency Myopathy with deficiency of succinate dehydrogenase and aconitase Creatine Amish nemaline myopathy Spheroid body myopathy Muscle-eye-brain disease Desmin-related myopathy Carnitine palmitoyltransferase 2 deficiency Central core myopathy Muscular dystrophy, late-onset distal Emery-Dreifuss muscular dystrophy, X-linked Short chain acyl-CoA dehydrogenase deficiency Plasma membrane carnitine transporter deficiency Carnitine deficiency myopathy Phosphogylcerate mutase 2 deficiency Vitamin D dependent rickets type 1 Congenital muscular dystrophy, autosomal recessive Glycogenosis type 2 amyloidosis.

MERRF MERRF MERRF syndrome, a mitochondrial disease wikipedia Barth syndrome Barth syndrome Barth syndrome, also known as 3-Methylglutaconic aciduria type II and Cardiomyopathy-neutropenia syndrome, a rare genetic disorder classified by many signs and symptoms, including metabolism distortion, delayed motor skills, stamina deficiency wikipedia Myotubular myopathy Myotubular myopathy centronuclear myopathy (Centronuclear myopathies, the group of congenital myopathies where cell nuclei, abnormally located in skeletal muscle cells) wikipedia Walker-Warburg syndrome Walker-Warburg syndrome Walker-Warburg syndrome, a rare form of autosomal recessive congenital muscular dystrophy associated with brain and eye abnormalities wikipedia Alpha-mannosidosis Alpha-mannosidosis Alpha-mannosidosis, an autosomal recessive metabolic disorder that causes mental and physical deterioration wikipedia Bethlem myopathy Bethlem myopathy Bethlem myopathy, a form of myopathy caused by a variation in one of the three genes coding for type VI collagen wikipedia glutaric acidemia type 2 glutaric acidemia type 2 Glutaric acidemia type 2, an autosomal recessive metabolic disorder that is characterised by defects in the ability of the body to use proteins and fats for energy wikipedia Clevudine Clevudine Clevudine, the antiviral drug for the treatment of hepatitis B wikipedia AIDS AIDS AIDS the event wikipedia ethanol ethanol, the alcohol found in alcoholic beverages, also known as ethyl alcohol or grain alcohol wikipedia Atorvastatin Atorvastatin, marketed under the trade name Lipitor among others, the member of the drug class known as statins, which are used primarily for lowering blood cholesterol and for prevention of events associated with cardiovascular disease wikipedia simvastatin simvastatin, a statin also sold as Zocor wikipedia pravastatin Pravastatin, the member of the drug class of statins, used in combination with diet, exercise, and weight loss for lowering cholesterol and preventing cardiovascular disease wikipedia Fanconi syndrome Fanconi Syndrome, a disorder in which the proximal tubular function of the kidney is impaired, resulting in decreased reabsorption of electrolytes and nutrients back into the bloodstream wikipedia Becker's muscular dystrophy Becker's muscular dystrophy, a X-linked recessive inherited disorder characterized by slowly progressive muscle weakness of the legs and pelvis wikipedia Limb-girdle muscular dystrophy Limb-girdle muscular dystrophy or Erb's muscular dystrophy, an autosomal class of muscular dystrophy that is similar but distinct from Duchenne muscular dystrophy and Becker's muscular dystrophy wikipedia Myoadenylate deaminase deficiency Myoadenylate deaminase deficiency, a recessive genetic metabolic disorder that affects approximately 1-2% of populations of European descent Bezafibrate Bezafibrate, the fibrate drug used for the treatment of hyperlipidaemia wikipedia nemaline myopathy nemaline myopathy, a congenital, hereditary neuromuscular disorder that causes muscle weakness, generally nonprogressive, of varying severity wikipedia Glycogen storage disease type III Glycogen storage disease type III, an autosomal recessive metabolic disorder and inborn error of metabolism, that is characterized by a deficiency in glycogen debranching enzymes wikipedia Distal muscular dystrophy Distal muscular dystrophy, a group of disorders characterized by onset in the hands or feet wikipedia Telbivudine Telbivudine, the antiviral drug used in the treatment of hepatitis B infection wikipedia hereditary inclusion body myopathy hereditary inclusion body myopathy (Hereditary inclusion body myopathies, the heterogeneous group of genetic disorders which have different symptoms) wikipedia Adducted thumb syndrome Adducted thumb syndrome recessive form, also known as Christian syndrome or Craniostenosis arthrogryposis cleft palate, a rare disease affecting multiple systems which causes malformations of the palate, thumbs, and upper limbs wikipedia Myoneurogenic gastrointestinal encephalopathy Myoneurogenic gastrointestinal encephalopathy or MNGIE, a rare mitochondrial disease typically appearing between the second and fifth decades of life wikipedia Fukuyama congenital muscular dystrophy Fukuyama congenital muscular dystrophy, a form of muscular dystrophy mainly described in Japan wikipedia mitochondrial trifunctional protein deficiency Mitochondrial trifunctional protein deficiency, an autosomal recessive fatty acid oxidation disorder that prevents the body from converting certain fats to energy, particularly during periods without food wikipedia Triosephosphate isomerase deficiency Triosephosphate isomerase deficiency, a rare, autosomal recessive disorder which, initially described in 1965 wikipedia Ullrich congenital muscular dystrophy Ullrich congenital muscular dystrophy, the form of congenital muscular dystrophy wikipedia Marinesco-Sjogren syndrome Marinesco-Sjogren syndrome, a rare autosomal recessive disorder wikipedia Chanarin-Dorfman disease Neutral lipid storage disease, the autosomal recessive disorder characterized by accumulation of triglycerides in the cytoplasm of leukocytes, muscle, liver, fibroblasts, and other tissues wikipedia Glycerol kinase deficiency Hyperglycerolemia, also referred to as "glycerol kinase deficiency", "gk deficiency", "gkd", and "gk1 deficiency", the condition characterized by high levels of glycerides, including monoglycerides, diglycerides and triglycerides, in the blood stream wikipedia Emery-Dreifuss muscular dystrophy type 2 Emery-Dreifuss muscular dystrophy type 2, the cause and medical condition with Mesh code "D020389" and DiseasesDB code "31705" Tel Hashomer camptodactyly syndrome Tel Hashomer camptodactyly syndrome, the cause and medical concept with DiseasesDB code "33498" Rigid spine muscular dystrophy type 1 Rigid spine muscular dystrophy type 1, the cause and medical concept with DiseasesDB code "33506" Myotubular myopathy, X-linked Myotubular myopathy, X-linked (an X-linked form of myotubular myopathy) Carey-Fineman-Ziter syndrome Carey-Fineman-Ziter syndrome, the cause and medical condition with DiseasesDB code "33758" X-linked myopathy with excessive autophagy X-linked myopathy with excessive autophagy, the cause and medical concept with DiseasesDB code "33762" Calpainopathy Calpainopathy, the cause and medical concept with DiseasesDB code "33979" Very long-chain acyl-CoA dehydrogenase deficiency Very long-chain acyl-CoA dehydrogenase deficiency, the cause and medical concept with DiseasesDB code "34113" Myosin storage myopathy Myosin storage myopathy, the cause and medical condition with DiseasesDB code "34301" Congenital fiber-type disproportion myopathy Congenital fiber-type disproportion myopathy, the cause and medical concept with Mesh code "D020914" and DiseasesDB code "34354" Progressive external ophthalmoplegia, autosomal recessive Progressive external ophthalmoplegia, autosomal recessive, the cause and medical condition with DiseasesDB code "34661" Neutral lipid storage disease with myopathy Neutral lipid storage disease with myopathy, the cause and medical concept with DiseasesDB code "34670" Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia, the cause and medical concept with DiseasesDB code "34680" Lactate dehydrogenase-A deficiency Lactate dehydrogenase-A deficiency, the cause and medical concept with DiseasesDB code "34717" Myopathy with deficiency of succinate dehydrogenase and aconitase Myopathy with deficiency of succinate dehydrogenase and aconitase, the cause and medical concept with DiseasesDB code "34719" Creatine Creatine, the chemical compound, a cause of the phenomenon lung cancer and rhabdomyolysis Amish nemaline myopathy Amish nemaline myopathy, the cause and medical concept with DiseasesDB code "33447" Spheroid body myopathy Spheroid body myopathy, the cause and medical concept with DiseasesDB code "33250" Muscle-eye-brain disease Muscle-eye-brain disease (a pachygyria-polymicrogyria syndrome with many features overlapping those of Walker-Warburg and cerebro-oculo-muscular syndromes) Desmin-related myopathy Desmin-related myopathy, the cause and medical concept with DiseasesDB code "32562" Carnitine palmitoyltransferase 2 deficiency Carnitine palmitoyltransferase 2 deficiency, the cause and medical concept with DiseasesDB code "32534" Central core myopathy Central core myopathy (an inherited congenital myopathic condition characterized by weakness and hypotonia in infancy and delayed motor development) Muscular dystrophy, late-onset distal Muscular dystrophy, late-onset distal, the cause and medical concept with DiseasesDB code "31977" Emery-Dreifuss muscular dystrophy, X-linked Emery-Dreifuss muscular dystrophy, X-linked, the cause and medical concept with Mesh code "D020389" and DiseasesDB code "31704" Short chain acyl-CoA dehydrogenase deficiency Short chain acyl-CoA dehydrogenase deficiency, the cause and medical concept with DiseasesDB code "31599" Plasma membrane carnitine transporter deficiency Plasma membrane carnitine transporter deficiency, the cause and medical concept with DiseasesDB code "31103" Carnitine deficiency myopathy Carnitine deficiency myopathy (rare genetic carnitine metabolic disorder that causes extreme muscle weakness; carnitine functions in the body as a carrier of fatty acids to the energy centers in muscles (mitochondria)) Phosphogylcerate mutase 2 deficiency Phosphogylcerate mutase 2 deficiency, the cause and medical concept with DiseasesDB code "30074" Vitamin D dependent rickets type 1 Vitamin D dependent rickets type 1, the cause and medical concept with DiseasesDB code "4737" Congenital muscular dystrophy, autosomal recessive Congenital muscular dystrophy, autosomal recessive, the cause and medical concept with DiseasesDB code "3061" Glycogenosis type 2 Glycogenosis type 2 (an autosomal recessively inherited glycogen storage disease caused by glucan 1,4-alpha-glucosidase deficiency) amyloidosis Amyloidosis (any disease manifested by the pathogenic accumulation of amyloid in organs and tissues).

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