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148 Possible Causes for Loss of Motor Skills, Myopathy, Rhabdomyolysis

  • Duchenne Muscular Dystrophy

    […] of motor skills development fatigue rapidly worsening weakness in the legs, pelvis, arms, and neck DMD is a genetic disease.[] DMD is usually a challenge for the anaesthesiologist, with poor cardiac function, a high risk of developing rhabdomyolysis, and the probable life-threatening complications[] It is associated with a wide variety of myopathic disorders that affect paraspinal muscles, including inflammatory and inherited myopathies.[]

  • Chronic Alcoholism

    skills, or slurred speech.[] Of five chronic alcoholics with acute skeletal muscle necrosis (rhabdomyolysis) three developed acute heart failure with disturbances of rhythm and conduction.[] A patient with hypokalemic myopathy occurring in the context of chronic alcoholism was reported.[]

  • Tropical Myositis

    Affected infants lose motor skills such as turning over, sitting, and crawling. They also develop an exaggerated startle reaction to loud noises.[] DIAGNOSIS Tropical pyomyositis Rhabdomyolysis AKI HIV 13. Inj.Cloxacillin Clindamycin 14.[] Other parasitic myopathies such as trichinosis and cysticercosis are acquired through consumption of poorly cooked meats.[]

  • MELAS Syndrome

    Altered consciousness Motor skills loss Intellectual disability Causes MELAS syndrome is triggered by transmutations in the gene material – DNA – in the mitochondria.[] Furthermore, this mutation was associated with exercise-induced rhabdomyolysis, hearing loss, seizures, cardiomyopathy, and autism in the large kindred.[] Abstract Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome is a rare neurodegenerative disease caused by the decreased ability[]

  • Becker Muscular Dystrophy

    GENE INCLUDED: DMD INDICATIONS FOR TESTING: Developmental delay Gross motor delay or loss of motor skills Low muscle tone Calf hypertrophy Abnormal gait Dilated cardiomyopathy[] One patient with undiagnosed BMD received succinylcholine and developed acute rhabdomyolysis and hyperkalemic cardiac arrest.[] In a boy with myopathy and an increase of muscle fibres with central nuclei we detected a heterozygous 387G-- T nucleotide transversion in the MYF6 gene (MIM*159991).[]

  • Long Chain Hydroxyacyl-CoA Dehydrogenase Deficiency

    Babies and children who are not treated may have: poor weight gain delays in learning delays in walking and other motor skills enlarged liver and other liver problems enlarged[] These long chain defects have variable presentations, they may present in the neonate or infant with sudden death, hepatopathy (Reyes disease), hypoketotic hypoglycaemia, rhabdomyolysis[] Deficiencies of human β-oxidation enzymes produce sudden, unexplained death in childhood, acute hepatic encephalopathy, skeletal myopathy, or cardiomyopathy.[]

  • Combined Oxidative Phosphorylation Defect Type 14

    The gradual cumulative effects of these episodes often result in variable combinations of loss of motor skills (speech, movement, and eating), impaired sensation (vision loss[] It shares many features of MCADD, but patients may also have cardiomyopathy; rhabdomyolysis, massive creatine kinase elevations, and myoglobinuria with muscle exertion; peripheral[] Recessive hypomorphic ISCU alleles have been associated with isolated myopathy 11 12 or skeletal and cardiac myopathy 14 in humans.[]

  • Carcinomatous Myopathic Syndrome

    Myelopathy symptoms may include: Neck, arm, leg or lower back pain Tingling, numbness or weakness Difficulty with fine motor skills, such as writing or buttoning a shirt Increased[] […] phosphokinase test Electromyography Eyelid twitch Hypotonia Muscle aches Muscle atrophy Muscle biopsy Muscle function loss Muscle twitching Myopathic changes Myotonia congenita Rhabdomyolysis[] English Definition Of Carcinomatous Myopathy The word Carcinomatous Myopathy is a noun 1.[]

  • Episodic Mitochondrial Myopathy - Optic Atrophy - Reversible Leukoencephalopathy

    The gradual cumulative effects of these episodes often result in variable combinations of loss of motor skills (speech, movement, and eating), impaired sensation (vision loss[] Rhabdomyolysis was diagnosed and the patient was admitted for intravenous fluid hydration.[] Mitochondrial myopathies are types of myopathies associated with mitochondrial disease.[]

  • Proximal Myopathy with Extrapyramidal Signs

    This new rare disorder is characterized by normal early development followed by a progressive loss of mental and motor skills.[] For example, rhabdomyolysis (acute muscle breakdown) can lead to kidney problems by causing a protein called myoglobin to leak from ruptured muscle cells into the urine.[] MalaCards based summary : Myopathy with Extrapyramidal Signs, is also known as proximal myopathy with extrapyramidal signs, and has symptoms including tremor and involuntary[]

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