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5,091 Possible Causes for Cardiomyopathy, Persistent Notochordal Canal, Proximal Muscle Weakness Limb Girdle Distribution

  • Limb-Girdle Muscular Dystrophy

    This is the first report showing the electron microscopic findings of dilated cardiomyopathy (DCM) accompanied with limb girdle muscular dystrophy.[ncbi.nlm.nih.gov] LGMD2A type is also known as Calpainopathy, which is characterized by selective atrophy and weakness of proximal limb muscles.[ncbi.nlm.nih.gov] This may manifest as hypertrophic/dilated cardiomyopathy and cardiac dysrhythmias.[circheartfailure.ahajournals.org]

    Missing: Persistent Notochordal Canal
  • Emery-Dreifuss Muscular Dystrophy Type 1

    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] ) • Progressive atrophy of humero-peroneal distribution (proximal muscles of upper limb and distal muscles of lower limb).[physio-pedia.com] […] 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]

    Missing: Persistent Notochordal Canal
  • Emery-Dreifuss Muscular Dystrophy Type 2

    An Indian family with an Emery-Dreifuss myopathy and familial dilated cardiomyopathy due to a novel LMNA mutation.[annalsofian.org] ) • Progressive atrophy of humero-peroneal distribution (proximal muscles of upper limb and distal muscles of lower limb).[physio-pedia.com] 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]

    Missing: Persistent Notochordal Canal
  • Limb-Girdle Muscular Dystrophy Type 2J

    Disease Type of connection Familial isolated dilated cardiomyopathy Autosomal recessive centronuclear myopathy Early-onset myopathy with fatal cardiomyopathy Familial isolated[csbg.cnb.csic.es] notochordal canal syndrome Salla disease Salt-and-pepper syndrome Sandhoff disease Sandhoff disease, adult form Sandhoff disease, infantile form Sandhoff disease, juvenile[se-atlas.de] LGMD1B patients often exhibit findings of both cardiomyopathy and dysrhythmia [ 7 ].[pubs.sciepub.com]

    Missing: Proximal Muscle Weakness Limb Girdle Distribution
  • 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[ncbi.nlm.nih.gov] ) • Progressive atrophy of humero-peroneal distribution (proximal muscles of upper limb and distal muscles of lower limb).[physio-pedia.com] […] have diagnostic/prognostic value in heart diseases, it is worth assessing whether it is also involved in the pathogenesis and can be applied in the diagnosis of the dilated cardiomyopathy[ncbi.nlm.nih.gov]

    Missing: Persistent Notochordal Canal
  • Alpha-B Crystallinopathy

    Secondary cardiomyopathies are those in which the cardiomyopathy is found in a systemic disease.[intechopen.com] notochordal canal syndrome Salla disease Salt-and-pepper syndrome Sandhoff disease Sandhoff disease, adult form Sandhoff disease, infantile form Sandhoff disease, juvenile[se-atlas.de] , Dilated, 1A Cardiomyopathy, Congestive Cardiomyopathy, Dilated, With Conduction Defect 1 Cardiomyopathy, Familial Idiopathic Cardiomyopathy, Idiopathic Dilated CMD1A CDCD1[ukgtn.nhs.uk]

    Missing: Proximal Muscle Weakness Limb Girdle Distribution
  • Congenital Muscular Dystrophy due to LMNA Mutation

    […] laminopathy Autosomal dominant limb-girdle muscular dystrophy type 1B Autosomal recessive Emery-Dreifuss muscular dystrophy Charcot-Marie-Tooth disease type 2B1 Dilated cardiomyopathy[csbg.cnb.csic.es] Contracture involvement is not an early sign and is often mild in LGMD1B. 5 The pattern of muscle involvement is also milder in LGMD1B, with a proximal limb-girdle distribution[pc.thejcn.com] Keywords: Lamin A/c Lmna / Arrhythmia / Automatic Implantable Cardiac Defibrillator / cardiomyopathy / congenital muscular dystrophy Click here to see the statistics on "[scilit.net]

    Missing: Persistent Notochordal Canal
  • Nemaline Myopathy

    The combination of nemaline myopathy and cardiomyopathy is rare, and this is the first reported case of dilated cardiomyopathy associated with childhood-onset nemaline myopathy[ncbi.nlm.nih.gov] notochordal canal syndrome Salla disease Salt-and-pepper syndrome Sandhoff disease Sandhoff disease, adult form Sandhoff disease, infantile form Sandhoff disease, juvenile[se-atlas.de] The approach to determining an etiology for hypertrophic cardiomyopathy in an infant is reviewed.[ncbi.nlm.nih.gov]

    Missing: Proximal Muscle Weakness Limb Girdle Distribution
  • Malnutrition

    Carnitine nutritional deficiency Decreased nutritional requirement Deficiency of macronutrients Deficiency of micronutrients Dietary potassium - low Dietary sodium - low Dilated cardiomyopathy[icd9data.com] Explore the full collection Clinical presentation and survival of childhood hypertrophic cardiomyopathy: a retrospective study in United Kingdom Full text article Myocardial[oxfordjournals.org] Find out more Cancer therapy-induced cardiomyopathy: can human induced pluripotent stem cell modelling help prevent it?[oxfordjournals.org]

    Missing: Persistent Notochordal Canal Proximal Muscle Weakness Limb Girdle Distribution
  • Chronic Alcoholism

    […] without cardiomyopathy (p 0.001, both) and controls (p 0.05, both).[ncbi.nlm.nih.gov] Light-to-moderate alcohol intake is associated with a decreased incidence of coronary heart disease, while heavy drinking may be a precursor for cardiomyopathy.[symptoma.com] Cardiomyopathy was defined according to standard functional and histological criteria.[ncbi.nlm.nih.gov]

    Missing: Persistent Notochordal Canal Proximal Muscle Weakness Limb Girdle Distribution

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