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5,044 Possible Causes for Loss of Ambulation between Third and Sixth Decade, No Cardiomyopathy, 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]

  • 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: Loss of Ambulation between Third and Sixth Decade
  • 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: Loss of Ambulation between Third and Sixth Decade
  • Heelspur

    Female infant with oncocytic cardiomyopathy and microphthalmia with linear skin defects (MLS): a clue to the patho genesis of oncocytic cardiomyopathy?[journals.sagepub.com] ), focal lipid cardiomyopathy (Bove and Schwartz, 1973), oncocytic cardiomyopathy (Silver et al., 1980), infantile cardiomyopathy with histiocytoid change (Ferrans et al.,[malacards.org] […] arrhythmias or dilated cardiomyopathy.[ncbi.nlm.nih.gov]

    Missing: Loss of Ambulation between Third and Sixth Decade Persistent Notochordal Canal
  • Heart Failure

    Predisposing factors for CQ/HCQ-induced cardiomyopathy have been proposed.[ncbi.nlm.nih.gov] Few cases report patients with heart failure, secondary to dilated cardiomyopathy, with high fever.[ncbi.nlm.nih.gov] Abstract Isolated ventricular noncompaction, a rare genetic cardiomyopathy, is thought to be caused by the arrest of normal myocardial morphogenesis.[ncbi.nlm.nih.gov]

    Missing: Loss of Ambulation between Third and Sixth Decade Persistent Notochordal Canal
  • Congestive Heart Failure

    An 88-year-old man who had previously been diagnosed with apical hypertrophic cardiomyopathy exhibited left ventricular asynergy on echocardiography before undergoing cholecystectomy[ncbi.nlm.nih.gov] Immediate diagnosis and treatment are required for better control of acromegalic cardiomyopathy.[ncbi.nlm.nih.gov] Malnutrition Ischemia Diastolic ventricular dysfunction or failure may be caused by the following: Hypertrophic cardiomyopathy Restrictive cardiomyopathy Pericarditis Cardiac[emedicine.com]

    Missing: Loss of Ambulation between Third and Sixth Decade Persistent Notochordal Canal
  • Cardiomyopathy

    Those affected are at an increased risk of sudden cardiac death.Types of cardiomyopathy include hypertrophic cardiomyopathy, dilated cardiomyopathy, restrictive cardiomyopathy[en.wikipedia.org] Clinically, there are basically three types of cardiomyopathies: Restrictive, Dilated, and Hypertrophic cardiomyopathy.[symptoma.com] Other Names for Restrictive Cardiomyopathy Idiopathic restrictive cardiomyopathy Infiltrative cardiomyopathy What Causes Restrictive Cardiomyopathy Certain diseases, conditions[heart.org]

    Missing: Loss of Ambulation between Third and Sixth Decade Persistent Notochordal Canal
  • Left Cardiac Ventricle Disorder

    Restrictive Cardiomyopathy (RCM) Restrictive cardiomyopathy (RCM) is the least common type of cardiomyopathy accounting for only 5% of patients with cardiomyopathy.[childrenscardiomyopathy.org] Cardiomyopathy UK. April 2018.[cardiomyopathy.org] Takotsubo Cardiomyopathy Treatment There are no evidence-based guidelines for treating takotsubo cardiomyopathy.[health.harvard.edu]

    Missing: Loss of Ambulation between Third and Sixth Decade Persistent Notochordal Canal
  • Hypertrophic Cardiomyopathy

    What is hypertrophic cardiomyopathy?[symptoma.com] Codd MB, Sugrue DD, Gersh BJ, Melton LJ: Epidemiology of idiopathic dilated and hypertrophic cardiomyopathy.[doi.org] Hypertrophic cardiomyopathy. Prog Cardiovasc Dis. 1994;36:275-308. Google Scholar 11. Marian AJ, Roberts R.[doi.org]

    Missing: Loss of Ambulation between Third and Sixth Decade Persistent Notochordal Canal
  • Infantile-Onset Autosomal Recessive Nonprogressive Cerebellar Ataxia

    (familial) (idiopathic) I42.9 ICD-10-CM Diagnosis Code I42.9 Cardiomyopathy, unspecified 2016 2017 2018 2019 Billable/Specific Code Applicable To Cardiomyopathy (primary)[icd10data.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] […] associated with vitamin E deficiency Kearns-Sayre syndrome (sporadic) MtDNA deletion and duplication mutations Ptosis, ophthalmoplegia, pigmentary retinal degeneration, cardiomyopathy[bcm.edu]

    Missing: Loss of Ambulation between Third and Sixth Decade

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