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102 Possible Causes for Cardiomyopathy, Onset of Symptoms in First or Second Decade of Life

  • Limb-Girdle Muscular Dystrophy Type 2E

    The onset of symptoms usually occurs in the first or second decade of life. Affected individuals usually present with impairment of upper extremity elevation.[icd10data.com] LGMD1B patients often exhibit findings of both cardiomyopathy and dysrhythmia [ 7 ].[pubs.sciepub.com] Calf hypertrophy, cardiomyopathy, respiratory impairment, tendon contractures, scoliosis, and exercise-induced myoglobinuria may be observed.[rarediseases.info.nih.gov]

  • Limb-Girdle Muscular Dystrophy Type 2F

    The onset of symptoms usually occurs in the first or second decade of life. Affected individuals usually present with impairment of upper extremity elevation.[icd10data.com] Keywords Delta-sarcoglycan Severe LGMD phenotype Cardiomyopathy References 1. Nigro V, Moreira ES, Piluso G, et al.[link.springer.com] LGMD1B patients often exhibit findings of both cardiomyopathy and dysrhythmia [ 7 ] .[pubs.sciepub.com]

  • Muscular Dystrophy-Dystroglycanopathy Type C5

    The onset of symptoms usually occurs in the first or second decade of life. Affected individuals usually present with impairment of upper extremity elevation.[icd10data.com] LGMD1B patients often exhibit findings of both cardiomyopathy and dysrhythmia [ 7 ].[pubs.sciepub.com] […] nonischemic cardiomyopathies (Figure 1 ).[jcmr-online.biomedcentral.com]

  • Limb-Girdle Muscular Dystrophy Type 2C

    The onset of symptoms usually occurs in the first or second decade of life. Affected individuals usually present with impairment of upper extremity elevation.[icd10data.com] Symptoms may additionally include: enlargement (hypertrophy) of the calf muscle and tongue, diseases of the heart muscle ( cardiomyopathy ), and respiratory abnormalities.[rarediseases.info.nih.gov] LGMD1B patients often exhibit findings of both cardiomyopathy and dysrhythmia [ 7 ].[pubs.sciepub.com]

  • Emery-Dreifuss Muscular Dystrophy Type 2

    The onset of symptoms usually occurs in the first or second decade of life. Affected individuals usually present with impairment of upper extremity elevation.[icd10data.com] An Indian family with an Emery-Dreifuss myopathy and familial dilated cardiomyopathy due to a novel LMNA mutation.[annalsofian.org] The frequency of familial dilated cardiomyopathy in a series of patients with idiopathic dilated cardiomyopathy. N Engl J Med 1992 ;326: 77 - 82 5.[nejm.org]

  • Emery-Dreifuss Muscular Dystrophy Type 1

    The onset of symptoms usually occurs in the first or second decade of life. Affected individuals usually present with impairment of upper extremity elevation.[icd10data.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]

  • Limb-Girdle Muscular Dystrophy

    The onset of symptoms usually occurs in the first or second decade of life. Affected individuals usually present with impairment of upper extremity elevation.[icd10data.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]

  • Congenital Muscular Dystrophy

    The onset of symptoms usually occurs in the first or second decade of life. Affected individuals usually present with impairment of upper extremity elevation.[icd10data.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]

  • Friedreich Ataxia

    Most affected people become wheelchair dependent by the second or third decade of life.[web.archive.org] They may develop a cardiomyopathy (CM) phenotype, which is similar to hypertrophic cardiomyopathy and potentially progresses towards a life-limiting problem.[escardio.org] Frataxin replacement and anti-inflammatory agents are potential therapies in FA cardiomyopathy.[ncbi.nlm.nih.gov]

  • Facioscapulohumeral Muscular Dystrophy

    Symptoms Symptom onset usually occurs during the second decade of life, rarely in infancy or adulthood. Facial muscles are affect first.[symptoma.com] This is the first report of an FSHD patient with biopsy-proven cardiomyopathy.[ncbi.nlm.nih.gov] Furthermore, the increased prevalence of incomplete RBBB in the absence of cardiomyopathy suggests a selective involvement of the His-Purkinje system in FSHD.[ncbi.nlm.nih.gov]

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