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412 Possible Causes for Cardiomyopathy, Progressive Contractures, Rhabdomyolysis

  • Chronic Alcoholism

    […] without cardiomyopathy (p 0.001, both) and controls (p 0.05, both).[] Acute renal failure secondary to progressively decreasing renal blood flow (hepatorenal syndrome) may develop.[] Of five chronic alcoholics with acute skeletal muscle necrosis (rhabdomyolysis) three developed acute heart failure with disturbances of rhythm and conduction.[]

  • Duchenne Muscular Dystrophy

    She was treated for peripartum cardiomyopathy (PPCM) with angiotensin converting enzyme inhibitors (ACEi), beta-blockers and diuretics with normalisation of her cardiac function[] Surgical Treatment Progressive contractures may be improved with tendon lengthening but recurrence rates may be high.[] DMD is usually a challenge for the anaesthesiologist, with poor cardiac function, a high risk of developing rhabdomyolysis, and the probable life-threatening complications[]

  • Glycogen Storage Disease

    We describe a 2-mo-old infant presenting with a familial form of GSD III complicated with cardiomyopathy.[] (40%): Shoulders; Hips; Knees; Neck Weight loss Smooth muscle: Urinary or Fecal incontinence Hearing loss Course Progressive Disability related to disease duration 14 Disability[] CK was mildly elevated at rest and over 20,000 U/L during her episode of rhabdomyolysis.[]

  • Dermatomyositis

    […] due to dermatomyositis Dilated cardiomyopathy secondary to dermatomyositis Disorder of respiratory system due to dermatomyositis Juvenile dermatomyositis Juvenile dermatomyositis[] , the muscles begin to waste away (atrophy) and permanently shorten (contracture); children with juvenile dermatomyositis may experience a more rapid onset.[] The laboratory results included an admission creatine phosphokinase of 9,508 U/L (reference range 21–232 U/L), which is consistent with rhabdomyolysis.[]

  • Alcoholic Myopathy

    Skip to Content « Previous Page En Español Alcoholic Cardiomyopathy Topic Overview Alcoholic cardiomyopathy is caused by long-term alcohol abuse.[] […] deformities may be present in addition to slowly progressive weakness.[] A 38-year-old man experienced six severe episodes of rhabdomyolysis and two episodes of pharyngeal muscle weakness superimposed on chronic alcoholic myopathy and complicated[]

  • Emery-Dreifuss Muscular Dystrophy

    Emery-Dreifuss muscular dystrophy: humeroperoneal muscular atrophy and weakness, neck and elbow contractures with sinus bradycardia, first-degree atrioventricular block, and dilated cardiomyopathy[] Abstract Emery-Dreifuss muscular dystrophy (EDMD) is a neuromuscular disorder resulting in progressive muscle weakness, contractures, and cardiomyopathy.[] The anaesthetic considerations for this syndrome are difficult tracheal intubation, difficult spinal anaesthetic, heart block, gastric reflux, rhabdomyolysis, and unproved[]

  • Congenital Muscular Dystrophy

    cardiomyopathy died at the ages of 2 years 1 month, and 7 years 4 months respectively.[] We report the first known Egyptian patient with FCMD, established by clinical features of generalized weakness, pseudohypertrophy of calf muscles, progressive joint contractures[] His acute rhabdomyolysis was possibly triggered by human parvovirus B19 infection. The Author(s) 2013.[]

  • Secondary Myopathy

    There are four types of non-ischemic cardiomyopathy: Dilated Cardiomyopathy Hypertrophic Cardiomyopathy Restrictive Cardiomyopathy Arrhythmogenic Right Ventricular Dysplasia[] Progressive contractures in hands, elbow, ankles and knees is progressive and patients usually do not attain ambulation. EOM and facial muscles are spared.[] Muscle manifestations in these categories include pathogen-caused myositis, muscle infarction, rhabdomyolysis, myasthenia, immune-mediated myositis, necrotising myopathy,[]

  • Autosomal Dominant Myoglobinuria

    Cardiomyopathy 1FF Dilated Cardiomyopathy 2A Familial Hypertrophic Cardiomyopathy 7 Familial Restrictive Cardiomyopathy TNNT2 Cardiac Troponin T2 Dilated Cardiomyopathy 1D[] There is variable rate of progression. May develop myalgia, myoglobinuria, contractures, muscle hypertrophy.[] , RHABDOMYOLYSIS, rhabdomyolysis, rhabdomyolysis (diagnosis), Rhabdomyolysis [Disease/Finding], Necrosis of skeletal muscle, Skeletal muscle necrosis, Necrosis of skeletal[]

  • Hereditary Myopathy with Lactic Acidosis due to ISCU Deficiency

    , dilated 1C, 601493 LMNA Cardiomyopathy, dilated, 1A, 115200 TTN Cardiomyopathy, dilated, 1G, 604145 BAG3 Cardiomyopathy, dilated, 1HH, 613881 DES Cardiomyopathy, dilated[] contractural syndrome 2 607598 190151 Autosomal recessive ERBB4 2q34 Amyotrophic lateral sclerosis 19 615515 600543 Autosomal dominant ERCC1 19q13.32 Cerebrooculofacioskeletal[] Triggers for Rhabdomyolysis Infection [ 95, 97 ].[]

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