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100 Possible Causes for Cardiomyopathy, Rapid Progression to Disability

  • Muscular Dystrophy

    It progresses slowly, with short periods of rapid muscle deterioration and weakness. Severity ranges from very mild to completely disabling.[webmd.com] A pilot study was conducted to assess the safety and efficacy of tranilast in muscular dystrophy patients with cardiomyopathy.[ncbi.nlm.nih.gov] Disease progression is typically very slow, with intermittent spurts of rapid muscle deterioration.[web.archive.org]

  • Duchenne Muscular Dystrophy

    Disease progression is typically very slow, with intermittent spurts of rapid muscle deterioration.[web.archive.org] She was treated for peripartum cardiomyopathy (PPCM) with angiotensin converting enzyme inhibitors (ACEi), beta-blockers and diuretics with normalisation of her cardiac function[ncbi.nlm.nih.gov] BACKGROUND: Duchenne muscular dystrophy (DMD) is frequently complicated by development of a cardiomyopathy.[ncbi.nlm.nih.gov]

  • Diffuse Scleroderma

    A rapid onset form of SYSTEMIC SCLERODERMA with progressive widespread SKIN thickening over the arms, the legs and the trunk, resulting in stiffness and disability.[connects.catalyst.harvard.edu] Severe organ involvement was defined as the presence of any of the following: 1) in the kidney, scleroderma "renal crisis"; 2) in the heart, cardiomyopathy, symptomatic pericarditis[ncbi.nlm.nih.gov] The effects of Scleroderma are progressive and tend to be disabling, and it is felt that early introduction of therapy may result in a better prognosis.[arthritis.co.za]

  • Emery-Dreifuss Muscular Dystrophy Type 1

    It progresses slowly, with short periods of rapid muscle deterioration and weakness. Severity ranges from very mild to completely disabling.[webmd.com] Abstract The original Virginia family with X‐linked muscular dystrophy with early contractures and cardiomyopathy (Emery‐Dreifuss type) has been reinvestigated 25 years later[doi.org] […] elbow, and neck tendons, beginning during early childhood and leading to limited joint movement; and cardiac anomalies (conduction defects, rhythm disturbances, and dilated cardiomyopathy[link.springer.com]

  • Primary Amyloidosis

    AL amyloidosis is a seriously disabling, progressive, and incurable condition. It is usually fatal within 1 to 2 years of diagnosis.[federalregister.gov] Abstract Cardiac amyloidosis is an infiltrative cardiomyopathy with a grave prognosis.[ncbi.nlm.nih.gov] The commonest form of cardiovascular manifestation is congestive heart failure due to restrictive cardiomyopathy caused by extensive interstitial infiltration of amyloid into[ncbi.nlm.nih.gov]

  • Limb-Girdle Muscular Dystrophy

    It progresses slowly, with short periods of rapid muscle deterioration and weakness. Severity ranges from very mild to completely disabling.[webmd.com] This is the first report showing the electron microscopic findings of dilated cardiomyopathy (DCM) accompanied with limb girdle muscular dystrophy.[ncbi.nlm.nih.gov] This may manifest as hypertrophic/dilated cardiomyopathy and cardiac dysrhythmias.[circheartfailure.ahajournals.org]

  • Systemic Scleroderma

    The effects of Scleroderma are progressive and tend to be disabling, and it is felt that early introduction of therapy may result in a better prognosis.[arthritis.co.za] , rare rheumatologic disease, lung disease, autoimmune cardiomyopathy Authority control Q5340515 Reasonator Scholia Statistics Subcategories This category has the following[commons.wikimedia.org] […] creatinine levels, and fibrosis on chest radiography. [2] The most common cause of early death in patients with juvenile systemic sclerosis is heart failure due to dilated cardiomyopathy[emedicine.com]

  • Mucopolysaccharidosis

    In early adulthood, however, they manifested a rapid cognitive decline. Subsequent cranial MRI imaging revealed progressive brain iron accumulation in deep brain nuclei.[ncbi.nlm.nih.gov] Cardiac involvement is common in MPS patients and usually consists of progressive valvular thickening with incompetence and cardiomyopathy.[ncbi.nlm.nih.gov] […] mucopolysaccharidosis type VI) is a rare lysosomal storage disorder in which the pathologic storage of glycosaminoglycans in various tissues can lead to severe symptoms, including cardiomyopathy[ncbi.nlm.nih.gov]

  • Congenital Muscular Dystrophy

    It progresses slowly, with short periods of rapid muscle deterioration and weakness. Severity ranges from very mild to completely disabling.[webmd.com] cardiomyopathy died at the ages of 2 years 1 month, and 7 years 4 months respectively.[ncbi.nlm.nih.gov] , Congenital cataract and cardiomyopathy, Dilated cardiomyopathy (DCM), Myopathy, myofibrillar, Cataract 16, multiple types, Myopathy, myofibrillar, fatal infantile hypertonic[blueprintgenetics.com]

  • Facioscapulohumeral Muscular Dystrophy

    However, evidence suggests that the disease course is most frequently characterized by slow progression with short periods of rapid muscle deterioration.[rarediseases.org] This is the first report of an FSHD patient with biopsy-proven cardiomyopathy.[ncbi.nlm.nih.gov] It progresses slowly, with short periods of rapid muscle deterioration and weakness. Severity ranges from very mild to completely disabling.[webmd.com]

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