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25 Possible Causes for Cardiomyopathy, Muscle Biopsy showing Presence of Vacuoles

  • Glycogen Storage Disease Type 2

    , lysosomal disease with hypertrophic cardiomyopathy, glycogen storage disease with hypertrophic cardiomyopathy, lysosomal glycogen storage disease Prende il nome da Johannes[] Muscle biopsy in Pompe disease shows the presence of vacuoles that stain positively for glycogen.[] If left untreated, affected infants often die from hypertrophic cardiomyopathy during their first year of life.[]

  • Distal Myopathy Type 3

    Involvement of the heart consists of usually terminal cardiomyopathy.[] The electromyograhy (EMG) shows a myopatic pattern and the muscles biopsy reveals dystrophic changes without the presence of rimmed vacuoles 1,4.[] The cardiomyopathy phenotype is usually classified as dilated cardiomyopathy (DCM) but also ARVC and hypertrophic cardiomyopathies (HCM) have been described.[]

  • Hypokalemic Periodic Paralysis

    Gosselin-Badaroudine, Mohamed Boutjdir and Mohamed Chahine, Mutations in the Voltage Sensors of Domains I and II of Nav1.5 that are Associated with Arrhythmias and Dilated Cardiomyopathy[]

  • Cardiodysrhythmic Potassium-Sensitive Periodic Paralysis

    A family with Andersen-Tawil syndrome and dilated cardiomyopathy.[] In periodic paralysis muscle biopsy may show a wide range of abnormalities, vacuoles being more specifically linked to the disease.[] […] rupture - Dressler's syndrome Layers Pericardium Pericarditis ( Acute, Constrictive ) - Pericardial effusion - Cardiac tamponade - Hemopericardium Myocardium Myocarditis Cardiomyopathy[]

  • Myopathy, Endocrine

    […] myopathies and neuropathies, and to include more information on genetic aspects of neuromuscular diseases, quantitative electromyo graphic techniques, plexus and root lesions and cardiomyopathies[] Muscle biopsy shows inflammation of muscle, fibre necrosis and the presence of vacuoles and filamentous inclusions in fibres (seen by electron microscopy).[] Usual onset between 3 and 5 years Clinical features Proximal muscles and neck flexors involved early Calf hypertrophy, Gower’s sign Contractures in tendoachilles, scoliosis, cardiomyopathy[]

  • Inclusion Body Myopathy

    Echocardiogram revealed a cardiomyopathy in both patients. This is the first report of the association between HIBM/DMRV and cardiomyopathy.[] Muscle biopsy will also show rimmed vacuoles (abnormal cellular structures that are also called inclusion bodies), amyloid deposits (presence of abnormal proteins), and endomysial[] Myofibrillar Myopathy With Arrhythmogenic Right Ventricular Cardiomyopathy. Desmin-Related Myopathy With Arrhythmogenic Right Ventricular Cardiomyopathy.[]

  • Fingerprint Body Myopathy

    Sengel and Stoebner found fingerprint bodies in the muscle of 5 adults; 2 had emphysema and the others had a progressive myopathy, cardiomyopathy, myotonic dystrophy , or[] Interattack muscle biopsies show the presence of single or multiple centrally placed vacuoles or tubular aggregates.[] Other associations are kyphoscoliosis or lordosis, foot deformities, congenital hip dislocations, contractures, hypertrophic cardiomyopathy, and arrythmias.[]

  • Proximal Myopathy with Extrapyramidal Signs

    […] w/ rhythm disturbance Unexplained heart block in a child Cardiomyopathy w/ lactic acidosis Dilated cardiomyopathy w/ muscle weakness Wolff-Parkinson-White arrhythmia Ophthalmologic[] Muscle biopsy shows the presence of vacuoles, containing glycogen, in muscle fibers, which are present during an attack, and which may decrease in number immediately after[] The concurrence of hypertrophic cardiomyopathy, arthrogryposis, and myopathy with muscle spindle excess suggests the presence of a newly described syndrome.[]

  • Inclusion Body Myositis

    We report the case of a patient with biopsy-proven IBM who developed heart failure and major ventricular arrhythmias secondary to dilated cardiomyopathy few months after the[] Muscle biopsy will also show rimmed vacuoles (abnormal cellular structures that are also called inclusion bodies), amyloid deposits (presence of abnormal proteins), and endomysial[] In this paper, we describe the autopsy findings of a patient with inclusion body myositis and hypertrophic cardiomyopathy.[]

  • Oculopharyngeal Muscular Dystrophy

    Cardiomyopathy or cardiac conduction defects have not been reported frequently.[] Muscle biopsy in the four affected patients showed variation in fiber size, and the presence of small angulated fibers and occasional rimmed vacuoles.[] Oculopharyngodistal myopathy - a possible association with cardiomyopathy. Neuromuscul Disord. 2011;21:121-5. [ Links ] 6 Pellerin HG, NicoTrépanier CA, Lessard MR.[]

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