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15 Possible Causes for Heart Disease, Mutation in the CALM2 Gene

  • Long QT Syndrome

    Patreon Help with Search Health Conditions and Diseases Cardiovascular Disorders Heart Disease Arrhythmia Long QT Syndrome 0 Long QT syndrome is a cardiac ion channel disease[curlie.org] RESULTS: A novel de novo CALM2 mutation (D132H) was discovered by candidate gene screening in a male infant with prenatal bradycardia born to healthy parents.[ncbi.nlm.nih.gov] There have been sporadic reports of LQTS coexisting with more common forms of congenital heart disease (CHD).[ncbi.nlm.nih.gov]

  • Ventricular Arrhythmia

    A total of 123 consecutive patients confirmed ischemia heart disease with ICD were examined.[ncbi.nlm.nih.gov] LQT15LQT15 is caused by heterozygous mutations in the CALM2 (Calmodulin 2) gene (114182) on chromosome 2p21.[en.wikipedia.org] Abstract Recurrent ventricular arrhythmias (VA) are a source of significant morbidity in patients without structural heart disease (SHD) and also mortality in patients with[ncbi.nlm.nih.gov]

  • Catecholaminergic Polymorphic Ventricular Tachycardia Type 2

    Linked Data Primary Entity # Electrical diseases of the heart.[worldcat.org] […] that have been discovered and only represent a small percentage of CPVT cases are TRDN (encoding triadin) and CALM1 (encoding calmodulin). 5,6 Mutations in the CALM2 gene[doi.org] Genetic variants of CPVT include RyR2, CASQ2, CALM2, TRD, and possibly KCNJ2 and ANK2 gene mutations.[ncbi.nlm.nih.gov]

  • Catecholaminergic Polymorphic Ventricular Tachycardia

    Australian Genetic Heart Disease Registry CPVT is one of the diseases being investigated by the Registry. We aim to enrol every family in Australia with CPVT.[heartregistry.org.au] RYR2, CASQ2, KCNJ2 , ANK2, CALM1, CALM2, TRDN, SCN5A* Other Panels that Include this Diagnosis Notes on Genes: Priority Genes: These genes include 70% of the mutations that[admerahealth.com] disease and high incidence of sudden cardiac death.[austinpublishinggroup.com]

  • Long QT Syndrome 15

    Congenital deaf mutism, functional heart disease with prolongation of the QT interval, and sudden death. Am Heart J. 1957;54:59-68. 4. Romano C, Gemme G, Pongiglione R.[revistas.uis.edu.co] heart disease: the ANOX study.[nsmc.hosp.go.jp] Braunwald’s Heart Disease , 7th ed, 2004. Philadelphia, PA: Elsevier Saunders, p. 689–95. 2. Moss AJ. Long QT Syndrome. In Podrid PJ, Kowey PR.[revistas.uis.edu.co]

  • Long QT Syndrome 13

    disease, atrial arrhythmias in congenital heart disease, and complications of catheter ablation of cardiac arrhythmias.[books.google.de] This prompted candidate-gene screening in a cohort of 82 LQTS genotype-negative patients. Two more patients were carriers of either CALM1 or CALM2 mutations.[smw.ch] Congenital deaf-mutism, functional heart disease with prolongation of the Q-T interval and sudden death. Am Heart J 1957;54:59-68.[acc.org]

  • Long QT Syndrome 10

    Conditions, SCD/Ventricular Arrhythmias, Atrial Fibrillation/Supraventricular Arrhythmias, Congenital Heart Disease, CHD and Pediatrics and Arrhythmias, CHD and Pediatrics[acc.org] This prompted candidate-gene screening in a cohort of 82 LQTS genotype-negative patients. Two more patients were carriers of either CALM1 or CALM2 mutations.[smw.ch] ICD-10-CM Codes › I00-I99 Diseases of the circulatory system › I30-I52 Other forms of heart disease › I45- Other conduction disorders › Long QT syndrome 2016 2017 2018 2019[icd10data.com]

  • Glycogen Storage Disease due to Muscle Phosphorylase Kinase Deficiency

    Prevention of coronary heart disease with pravastatin in men with hypercholesterolemia. ‎[books.google.es] There are autosomal recessive forms of GSD IX (caused by mutations in PHKB, PHKG1, PHKG2, CALM1, CALM2, and CALM3 ), a X-linked liver form (caused by mutations in PHKA2 ),[bmcmedgenet.biomedcentral.com] […] body they affect (like heart disease), mitochondrial diseases are so named because they affect a specific part of the cells in the body.[mda.org.nz]

  • Glycogen Storage Disease Type 9

    […] body they affect (like heart disease), mitochondrial diseases are so named because they affect a specific part of the cells in the body.[mda.org.nz] There are autosomal recessive forms of GSD IX (caused by mutations in PHKB, PHKG1, PHKG2, CALM1, CALM2, and CALM3 ), a X-linked liver form (caused by mutations in PHKA2 ),[bmcmedgenet.biomedcentral.com] Glycogen storage disease confined to the heart due to cardiac phosphorylase kinase deficiency causes a fatal infantile cardiomyopathy.[ncbi.nlm.nih.gov]

  • Jervell-Lange-Nielsen Syndrome

    Electrical heart disease: Genetic and molecular basis of cardiac arrhythmias in normal structural hearts.[litfl.com] A malignant form of LQTS associated to recurrent cardiac arrest due to VF in infants is associated to mutations in CALM1 and CALM2 genes encoding calmodulin (Crotti et al.[itaca.edu.es] Congenital deaf-mutism, functional heart disease with prolongation of the Q-T interval, and sudden death . Am Heart J 1957 ; 54 : 59 – 68 . 2.[cambridge.org]

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