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50 Possible Causes for Bilateral Congenital Profound Sensorineural Hearing Loss, Long QT Syndrome

  • Long QT Syndrome

    Although Long QT syndrome is often a genetic condition, a prolonged QT interval associated with an increased risk of abnormal heart rhythms can also occur in people without[en.wikipedia.org] 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] 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] […] interval with normal and prolonged QT intervals Diagnosing Long QT syndrome is challenging.[en.wikipedia.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] QT-interval.[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]

  • Congenital Deafness

    hearing loss ranges from mild to profound hearing loss.[wvdhhr.org] Abstract The Jervell and Lange Nielson syndrome(JLN) is an infrequent form of long QT syndrome (LQTS) in which prolonged QT interval and congenital deafness exist together[ncbi.nlm.nih.gov] Abstract Long QT syndrome (LQTS) is characterized by prolongation of the QT interval associated with a high risk for syncope and sudden death.[ncbi.nlm.nih.gov]

  • 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] Complications Most of the time, prolonged QT intervals in people with long QT syndrome never cause problems.[mayoclinic.org] […] congenital long QT syndrome.[anesthesiology.pubs.asahq.org]

  • 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] The electrocardiogram of these patients has a prominent U wave and a normal or modestly prolonged QT interval.[geneticheartdisease.org] Romano-Ward (prolonged QT interval) syndrome (I45.81) Jervell-Lange-Nielsen syndrome (I45.81) Equivalent ICD-9 Code GENERAL EQUIVALENCE MAPPINGS (GEM) Long QT syndrome (exact[icd.codes]

  • Jervell-Lange-Nielsen Syndrome Type 2

    The second symptom is a congenital bilateral profound sensorineural hearing loss.[hearinghealthmatters.org] Romano-Ward syndrome: Romano-Ward syndrome is the most common form of congenital long QT syndrome, which purely affects cardiac ion channels to produce prolonged QT interval[c-r-y.org.uk] 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]

  • 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] […] acquired long QT syndrome.[preventiongenetics.com] Congenital deaf-mutism, prolonged QT interval, syncopal attacks and sudden death.[litfl.com]

  • Autosomal Recessive Deafness 23

    […] born with profound congenital deafness.[vdocuments.site] PubMed CrossRef Google Scholar Keating, M., Genetics of the long QT syndrome. J. Cardiovasc. Electrophysiol. 5 (1994) 146–153.[link.springer.com] QT syndrome 4 Hereditary spherocytosis 1 Catenin APC Gardner's syndrome Familial adenomatous polyposis plakoglobin ( Naxos syndrome ) GAN ( Giant axonal neuropathy ) Other[en.wikipedia.org]

  • Autosomal Recessive Deafness 103

    PubMed CrossRef Google Scholar Keating, M., Genetics of the long QT syndrome. J. Cardiovasc. Electrophysiol. 5 (1994) 146–153.[link.springer.com] […] born with profound congenital deafness.[vdocuments.site] QT syndrome 4 Hereditary spherocytosis 1 Catenin APC Gardner's syndrome Familial adenomatous polyposis plakoglobin ( Naxos syndrome ) GAN ( Giant axonal neuropathy ) Other[en.wikipedia.org]

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