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myopathy

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myopathy
myopathy Path. (maɪˈɒpəθɪ) [ad. mod.L. myopathi-a: see myo- + -pathy.] Disease of the muscles. Hence myoˈpathic a.1849 Craig, Myopathy, a morbid condition of the muscles. 1856 Mayne Expos. Lex., Myopathicus,..of or belonging to Myopathia: myopathic. 1877 tr. von Ziemssen's Cycl. Med. XVI. 86 All the... Oxford English Dictionary
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Myopathy
Congenital myopathy with abnormal subcellular organelles Fingerprint body myopathy Inclusion body myopathy 2 Megaconial myopathy Myofibrillar myopathy Rimmed vacuolar myopathy Acquired (G72.0 - G72.2) External substance induced myopathy (G72.0) Drug-induced myopathy Glucocorticoid myopathy is caused wikipedia.org
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線維化筋症(Fibrotic Myopathy) ～ 後肢の機械性跛行を呈する疾患のひとつ | 水鳥や雉類の飼い方や知識
鬐甲瘻(Fistulous Withers) ～ 化膿性滲出物の漏出を呈する疾患. 感染性の棘上滑液嚢炎は、一般的に「鬐甲瘻：キ甲瘻（きこうろう）」と呼ばれ、棘上滑液包（馬の肩の部分とその関連組織）の皮膚が様々な量の壊死を伴って大量の漿...
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Congenital myopathy
One source includes nemaline myopathy, myotubular myopathy, central core myopathy, congenital fiber type disproportion, and multicore myopathy. Nemaline myopathy Nemaline myopathy was first described in 1963 and is the most common congenital myopathy. wikipedia.org
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Distal myopathy
Miyoshi myopathy affects the posterior muscles of the lower leg, more so than the anterior muscles of the lower leg. There are eight known types of distal myopathy. wikipedia.org
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Mitochondrial myopathy
It is now known that certain nuclear DNA deletions can also cause mitochondrial myopathy such as the OPA1 gene deletion. progressive external ophthalmoplegia (CPEO) Progressive ophthalmoparesis Symptomatic overlap with other mitochondrial myopathies Cause Mitochondrial myopathy wikipedia.org
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Metabolic myopathy
Diagnosis The symptoms of a metabolic myopathy can be easily confused with the symptoms of another disease. Some GSDs and a mitochondrial myopathy are known to have a pseudoathletic appearance. wikipedia.org
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Multi/minicore myopathy
Multi/minicore myopathy is a congenital myopathy usually caused by mutations in either the SEPN1 and RYR1 genes. It is also known as Minicore myopathy, Multicore myopathy, Multiminicore myopathy, Minicore myopathy with external ophthalmoplegia, Multicore myopathy wikipedia.org
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Bethlem myopathy
Bethlem myopathy is predominantly an autosomal dominant myopathy, classified as a congenital form of muscular dystrophy. Bethlem myopathy 1 (Collagen VI genes) See Bethlem myopathy 1 Clinical synopsis on OMIM: 158810 In Bethlem myopathy 1, in the calf, one of the first wikipedia.org
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非定型筋症(Atypical Myopathy) ～ 初期には嗜眠、食欲不振などの症状が見られる | 水鳥や雉類の飼い方や知識
鬐甲瘻(Fistulous Withers) ～ 化膿性滲出物の漏出を呈する疾患. 感染性の棘上滑液嚢炎は、一般的に「鬐甲瘻：キ甲瘻（きこうろう）」と呼ばれ、棘上滑液包（馬の肩の部分とその関連組織）の皮膚が様々な量の壊死を伴って大量の漿...
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Brody myopathy
Brody myopathy, also called Brody disease, is a rare disorder that affects skeletal muscle function. BD was first characterized in 1969 by Dr. Individuals with Brody myopathy also sometimes experience weakness, myalgia, and rhabdomyolysis. wikipedia.org
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Inflammatory myopathy
Inflammatory myopathy, also known as idiopathic inflammatory myopathy (IIM), is disease featuring muscle weakness, inflammation of muscles (myositis), myopathy. wikipedia.org
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Oculopharyngodistal myopathy
1; OPDM1: 37 families # 618940 OCULOPHARYNGODISTAL MYOPATHY 2; OPDM2: 30 families # 619473 OCULOPHARYNGODISTAL MYOPATHY 3; OPDM3: 11 families. See also Myopathy Familial episodic pain syndrome References Genetic diseases and disorders wikipedia.org
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Centronuclear myopathy
myopathy (CNM). (The terms "centronuclear myopathy" and "myotubular myopathy" are sometimes equated.) wikipedia.org
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Nemaline myopathy
Nemaline myopathy (also called rod myopathy or nemaline rod myopathy) is a congenital, often hereditary neuromuscular disorder with many symptoms that It is the most common non-dystrophic myopathy. "Myopathy" means muscle disease. wikipedia.org
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