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803 Possible Causes for Jervell-Lange-Nielsen Syndrome

  • Long QT Syndrome

    What is the treatment for Jervell-Lange-Nielsen syndrome?[californiaearinstitute.com] The two major forms are romano-ward syndrome and jervell-lange nielsen syndrome A ventricular arrhythmia characterized by syncopal episodes and a long qt interval, sometimes[icd9data.com] The population also contain individuals with the Swedish long QT syndrome (LQTS1) founder mutation ( KCNQ1 /p.Y111C) which in homozygotes causes the Jervell & Lange Nielsen[ncbi.nlm.nih.gov]

  • Long QT Syndrome 1

    Several missense variants are reported to cause RWS by a dominant-negative mechanism, and some KCNQ1 variants can cause both Jervell and Lange-Nielsen Syndrome (JLNS; in an[ncbi.nlm.nih.gov] "Jervell and Lange-Nielsen syndrome: a Norwegian perspective".[en.wikipedia.org] The Jervell and Lange-Nielsen syndrome: natural history, molecular basis and clinical outcome. Circulation 2006;113:783-790. 16. Zareba W, Goldenberg I, Moss AJ.[romanianjournalcardiology.ro]

  • Long QT Syndrome 6

    Jervell-Lange Nielsen syndrome in a family with the long QT syndrome (LQTS). Indian J Pediatr. 2007;74:90. author reply 90. PubMed 12.[springermedizin.de] The two major forms are romano-ward syndrome and jervell-lange nielsen syndrome.[icd10data.com] […] and Lange-Nielsen syndrome.[nejm.org]

  • Long QT Syndrome 10

    Jervell and Lange-Nielsen Syndrome is a similar disorder which is also associated with sensorineural hearing loss.[icd.codes] The two major forms are romano-ward syndrome and jervell-lange nielsen syndrome.[icd10data.com] (Medical Encyclopedia) [ Read More ] Jervell and Lange-Nielsen syndrome Jervell and Lange-Nielsen syndrome is a condition that causes profound hearing loss from birth and[icdlist.com]

  • Long QT Syndrome 14

    What is the treatment for Jervell-Lange-Nielsen syndrome?[californiaearinstitute.com] The two major forms are ROMANO-WARD SYNDROME and JERVELL-LANGE NIELSEN SYNDROME.[connects.catalyst.harvard.edu] Inheritance-Prototypes Autosomal dominant – Romano-Ward syndrome (RWS)  Autosomal recessive -Jervell and Lange-Nielsen syndrome (JLNS) 9.[de.slideshare.net]

  • Long QT Syndrome 13

    (LQT8), Timothy syndrome; 611818 (LQT9); 611819 (LQT10); 611820 (LQT11); 612955 (LQT12); 613485 (LQT13); 220400 Jervell and LangeNielsen syndrome 1, JLNS1; 612347 Jervell[nature.com] Romano-Ward Long QT Syndrome. In: NORD Guide to Rare Disorders. Lippincott Williams & Wilkins. Philadelphia, PA. 2003:54. Towbin JA. Jervell and Lange-Nielsen Syndrome.[rarediseases.org] Jervell and Lange-Nielsen syndrome: Jervell and Lange-Nielsen syndrome is a condition that causes profound hearing loss from birth, in addition to causing prolonged QT interval[c-r-y.org.uk]

  • Long QT Syndrome 8

    However, there are a few exceptions: patients with Timothy syndrome, patients with Jervell Lange-Nielsen syndrome carrying KCNQ1 mutations and LQT3 patients with 2:1 atrio-ventricular[ncbi.nlm.nih.gov] Jervell, Lange-Nielsen Syndrome (autosomal recessive inheritance pattern) – Both parents are carriers of the abnormal gene, but they may not manifest LQTS.[my.clevelandclinic.org] […] and Lange-Nielsen, 6 congenital long QT syndrome became an area of intensive research, and 25 years ago an international registry of patients and their families was established[mdedge.com]

  • Long QT Syndrome 5

    "Jervell and Lange-Nielsen syndrome: a Norwegian perspective".[en.wikipedia.org] The Jervell and Lange-Nielsen syndrome: natural history, molecular basis and clinical outcome. Circulation 2006;113:783-790. 16. Zareba W, Goldenberg I, Moss AJ.[romanianjournalcardiology.ro] […] and Lange-Nielsen syndrome.[en.wikipedia.org]

  • High Myopia-Sensorineural Deafness Syndrome

    Lange-Nielsen syndrome.[emedicine.medscape.com] , unilateral and bilateral, non-syndromic genetic deafness, Pendred syndrome, Usher syndrome, Stickler syndrome, Jervell and Lange-Nielsen syndrome, Mohr-Tranebjaerg syndrome[blueprintgenetics.com] […] loss: MTTS1 (tRNAser(UCN)), MTRNR1 (12S rRNA) Jervell and Lange-Nielsen syndrome: KCNQ1, KCNE1 Perrault syndrome: CLPP, HARS2, HSD17B4, LARS2 Alport syndrome: COL4A5, COL4A3[personalizedmedicine.partners.org]

  • Long QT Syndrome 3

    "Jervell and Lange-Nielsen syndrome: a Norwegian perspective".[en.wikipedia.org] The Jervell and Lange-Nielsen syndrome: natural history, molecular basis and clinical outcome. Circulation 2006;113:783-790. 16. Zareba W, Goldenberg I, Moss AJ.[romanianjournalcardiology.ro] Jervell A, Lange Nielsen F. Congenital deaf mutism, functional heart disease with prolongation of the QT interval, and sudden death. Am Heart J. 1957;54:59-68. 4.[revistas.uis.edu.co]

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