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30 Possible Causes for Bilateral Congenital Profound Sensorineural Hearing Loss, Ventricular Tachycardia

  • Long QT Syndrome

    The Jervell and Lange-Nielsen syndrome is an autosomal recessive form of LQTS and is characterized by congenital profound bilateral sensorineural hearing loss and long QT[medicinenet.com] Here we present a girl 20 months of age with refractory ventricular tachycardia due to long QT syndrome successfully treated by left cardiac sympathetic denervation.[ncbi.nlm.nih.gov] In some cases, LQTS may be associated with congenital profound bilateral sensorineural hearing loss, known as Jervell and Lange-Nielsen syndrome (JLNS).[mayomedicallaboratories.com]

  • Long QT Syndrome 6

    The Jervell and Lange-Nielsen syndrome is an autosomal recessive form of LQTS and is characterized by congenital profound bilateral sensorineural hearing loss and long QT[medicinenet.com] Patients with this condition tend to develop severe arrhythmias such as ventricular tachycardia, especially polymorphic ventricular tachycardia (VT) or torsade de pointes[omicsonline.org] In some cases, LQTS may be associated with congenital profound bilateral sensorineural hearing loss, known as Jervell and Lange-Nielsen syndrome (JLNS).[mayomedicallaboratories.com]

  • Long QT Syndrome 13

    The Jervell and Lange-Nielsen syndrome is an autosomal recessive form of LQTS and is characterized by congenital profound bilateral sensorineural hearing loss and long QT[medicinenet.com] Monitor revealed a wide complex, polymorphic ventricular tachycardia, which reverted to sinus rhythm in a span of few seconds.[jtd.amegroups.com] In some cases, LQTS may be associated with congenital profound bilateral sensorineural hearing loss, known as Jervell and Lange-Nielsen syndrome (JLNS).[mayomedicallaboratories.com]

  • Long QT Syndrome 10

    In some cases, LQTS may be associated with congenital profound bilateral sensorineural hearing loss, known as Jervell and Lange-Nielsen syndrome (JLNS).[mayomedicallaboratories.com] I47.0 Re-entry ventricular arrhythmia I47.1 Supraventricular tachycardia I47.2 Ventricular tachycardia Reimbursement claims with a date of service on or after October 1,[icd10data.com] Patients with this condition tend to develop severe arrhythmias such as ventricular tachycardia, especially polymorphic ventricular tachycardia (VT) or torsade de pointes[omicsonline.org]

  • Long QT Syndrome 8

    Jervell and Lange-Nielsen syndrome (JLNS) is characterized by congenital profound bilateral sensorineural hearing loss and LQTc usually greater than 500 msec.[ncbi.nlm.nih.gov] tachycardia.[mdedge.com] She had two appropriate AICD shocks that occurred within six months of implantation due to polymorphic ventricular tachycardia.[radcliffecardiology.com]

  • Jervell-Lange-Nielsen Syndrome Type 2

    The second symptom is a congenital bilateral profound sensorineural hearing loss.[hearinghealthmatters.org] Abstract A four-year-old deaf girl with a history of convulsions developed polymorphous ventricular tachycardia during induction of anaesthesia.[ncbi.nlm.nih.gov] It is characterized by congenital profound bilateral sensorineural hearing loss, a long QT interval, ventricular tachyarrhythmias, and episodes of torsade de pointes on an[ncbi.nlm.nih.gov]

  • Usher Syndrome Type 1H

    Usher syndrome type I is characterized by congenital, bilateral, profound sensorineural hearing loss, vestibular areflexia, and adolescent-onset retinitis pigmentosa.[ncbi.nlm.nih.gov] tachycardia Adeno-associated viral vector serotype 9 containing the human cardiac calsequestrin gene Treatment of plasma cell myeloma Marizomib Treatment for necrotising[elbiruniblogspotcom.blogspot.com] […] oligonucleotide directed against antithrombin mRNA and covalently linked to a ligand containing three N-acetylgalactosamine residues Treatment of catecholaminergic polymorphic ventricular[elbiruniblogspotcom.blogspot.com]

  • Jervell-Lange-Nielsen Syndrome

    It is characterized by congenital profound bilateral sensorineural hearing loss, a long QT interval, ventricular tachyarrhythmias, and episodes of torsade de pointes on an[jmedicalcasereports.biomedcentral.com] Keywords: Cervicothoracic sympathectomy, long QT syndrome, ventricular tachycardia How to cite this article: Roy PM, Khanna S, Mehta Y, Khan AZ.[ijaweb.org] Ventricular tachycardia with 2 variable opposing foci . Arch Mal Coeur Vaiss 1966 ; 59 : 263 – 272 . 10. Kleinman , CS , Glickstein , JS , Shaw , RF , et al .[cambridge.org]

  • Hereditary Hyperekplexia

    Tietz syndrome Tietz syndrome is a genetic hypopigmentation and deafness syndrome characterized by congenital profound bilateral sensorineural hearing loss and generalized[amp.pharm.mssm.edu] […] septal defect PS614429 Ventricular tachycardia, catecholaminergic polymorphic PS604772 Vesicoureteral reflux PS193000 Vitamin K-dependent clotting factors, combined deficiency[omim.org] tachycardia, idiopathic) GNAS (McCune-Albright syndrome) GNASAS (Pseudohypoparathyroidism, type IB) GNAT1 (Night blindness, congenital stationary, autosomal dominant 3) GNE[en.praenatal-medizin.de]

  • Autosomal Dominant Deafness 33

    […] born with profound congenital deafness.[docslide.net] Cardiac arrhythmias such as ventricular tachycardia and ventricular fibrillation are more common in mitral valve prolapse.[emedicine.medscape.com] tachycardia Congenital varicella syndrome Familial partial lipodystrophy Primary ciliary dyskinesia Watson syndrome Single upper central incisor Roch-Leri mesosomatous lipomatosis[checkrare.com]

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