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12 Possible Causes for Risk of Sudden Death due to Cardiac Defects

  • Emery-Dreifuss Muscular Dystrophy Type 1

    […] of sudden death due to cardiac defects; Female carriers may have cardiac defects MOLECULAR BASIS: Caused by mutations in the emerin gene (EMD, 300384 .0001) Contributors:[genome.jp] […] biopsy; Absence of emerin by immunohistochemistry on muscle biopsy; Increased serum creatine kinase MISCELLANEOUS: Onset in childhood; Adult onset has been rarely reported; Risk[genome.jp]

  • Congenital Muscular Dystrophy due to LMNA Mutation

    […] of sudden death due to cardiac defects; Female carriers may have cardiac defects MOLECULAR BASIS: Caused by mutations in the emerin gene (EMD, 300384 .0001) Contributors:[genome.jp] […] biopsy; Absence of emerin by immunohistochemistry on muscle biopsy; Increased serum creatine kinase MISCELLANEOUS: Onset in childhood; Adult onset has been rarely reported; Risk[genome.jp]

  • Autosomal Dominant Emery-Dreifuss Muscular Dystrophy

    […] of sudden death due to cardiac defects; Female carriers may have cardiac defects MOLECULAR BASIS: Caused by mutations in the emerin gene (EMD, 300384 .0001) Contributors:[genome.jp] […] biopsy; Absence of emerin by immunohistochemistry on muscle biopsy; Increased serum creatine kinase MISCELLANEOUS: Onset in childhood; Adult onset has been rarely reported; Risk[genome.jp]

  • Autosomal Dominant Emery-Dreifuss Muscular Dystrophy 2

    […] of sudden death due to cardiac defects; Female carriers may have cardiac defects MOLECULAR BASIS: Caused by mutations in the emerin gene (EMD, 300384 .0001) Contributors:[genome.jp] […] biopsy; Absence of emerin by immunohistochemistry on muscle biopsy; Increased serum creatine kinase MISCELLANEOUS: Onset in childhood; Adult onset has been rarely reported; Risk[genome.jp]

  • Costello Syndrome

    There is an increased risk of malignancies in these patients, due to the proto-oncogene mutation, and also sudden death secondary to heart disease.[ncbi.nlm.nih.gov] Clinical findings include facial dysmorphism, skin disorders, cognitive impairment, cardiac and musculoskeletal defects.[ncbi.nlm.nih.gov]

  • Normokalemic Periodic Paralysis

    -Due to the risk of life-threatening cardiac dysrhythmias and sudden death, must obtain immediate ECG* to ascertain if electrocardiac signs of electrolyte imbalances are[quizlet.com] **Hypotension, Dysrhythmias, ECG changes -(Tall (Peaked) T waves,* Absent P waves, Wide QRS, Prolonged QT interval, Sinus brady, conduction defects) Initial eval of hyperkalemia[quizlet.com]

  • Phentermine

    death due to cardiac arrhythmia in epilepsy patients [80] .[journals.lww.com] Topiramate is a pregnancy class D compound that carries teratogenic risk, specifically possible risk of craniofacial defects [65,66] .[journals.lww.com] Although in-vitro evidence has suggested the potential for topiramate to be arrhythmogenic [79] , data indicate that topiramate does not increase the risk of sudden unexpected[journals.lww.com]

  • Familial Thoracic Aortic Aneurysm 8

    Individuals with aortic aneurysms are at risk of sudden cardiac death due to rupture and dissection.[blueprintgenetics.com] […] in the Aorta Panel and their clinical significance Gene Associated phenotypes Inheritance ClinVar HGMD ABCC6 * Pseudoxanthoma elasticum AR 368 374 ABL1 Congenital heart defects[blueprintgenetics.com]

  • Aneurysm-Osteoarthritis Syndrome

    Individuals with aortic aneurysms are at risk of sudden cardiac death due to rupture and dissection.[blueprintgenetics.com] […] in the Aorta Panel and their clinical significance Gene Associated phenotypes Inheritance ClinVar HGMD ABCC6 * Pseudoxanthoma elasticum AR 368 374 ABL1 Congenital heart defects[blueprintgenetics.com]

  • Aortic Dilation

    Individuals with aortic aneurysms are at risk of sudden cardiac death due to rupture and dissection.[blueprintgenetics.com] […] in the Aorta Panel and their clinical significance Gene Associated phenotypes Inheritance ClinVar HGMD ABCC6 * Pseudoxanthoma elasticum AR 368 374 ABL1 Congenital heart defects[blueprintgenetics.com]

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