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64 Possible Causes for Bilateral Congenital Profound Sensorineural Hearing Loss, Heart Disease

  • 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] 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] In some cases, LQTS may be associated with congenital profound bilateral sensorineural hearing loss, known as Jervell and Lange-Nielsen syndrome (JLNS).[mayomedicallaboratories.com]

  • Tietz Syndrome

    From Wikidata Jump to navigation Jump to search monogenic disease that is characterized by congenital profound bilateral sensorineural hearing loss and generalized albino-like[wikidata.org] Chest pain in adults usually leads to a battery of tests to rule out heart disease.[jenlynn401.wordpress.com] Hearing loss is always bilateral, congenital, sensorineural and profound. Psychomotor development is normal.[orpha.net]

  • 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] Transthoracic echocardiography showed all heart chambers to be normally related, normal left ventricular systolic function, and no valvular heart disease.[innovationsincrm.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 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] Congenital Heart Disease , Vol. 8, Issue. 4, p. 352.[cambridge.org] 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 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] disease, atrial arrhythmias in congenital heart disease, and complications of catheter ablation of cardiac arrhythmias.[books.google.de] 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] Conditions, SCD/Ventricular Arrhythmias, Atrial Fibrillation/Supraventricular Arrhythmias, Congenital Heart Disease, CHD and Pediatrics and Arrhythmias, CHD and Pediatrics[acc.org] 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]

  • Alstrom Syndrome

    Hearing All subjects showed a bilateral symmetrical moderate to profound sensorineural hearing loss. The onset of hearing loss was either congenital or early childhood.[journal.frontiersin.org] Family history: one patient's brother died at the age of 2 years because of a congenital heart disease, and the second brother was diagnosed for the congenital organic heart[ncbi.nlm.nih.gov] To date, there have been no reports examining the echocardiographic features of Alström-related heart disease.[ncbi.nlm.nih.gov]

  • Usher Syndrome Type 1K

    Usher syndrome type I is characterized by congenital, bilateral, profound sensorineural hearing loss, vestibular areflexia, and adolescent-onset retinitis pigmentosa.[ncbi.nlm.nih.gov] It has also used in the treatment of mountain sickness, Ménières disease, increased intracranial pressure.[wikivisually.com] Diagnostic methods Clinical diagnosis is based on findings of bilateral sensorineural hearing loss (symmetric, congenital and profound for type 1, and moderate to severe with[orpha.net]

  • Congenital Deafness

    hearing loss ranges from mild to profound hearing loss.[wvdhhr.org] In a related anomaly, the CHARGE association (short-hand for "Coloboma, Heart disease, choanal Atresia, Retarded development, Genital hypoplasia, Ear anomalies") features[symptoma.com] Heart Disease Any history of any type of heart condition needs to be disclosed (including past heart attacks).[1cover.co.nz]

  • Microtia

    […] canals, and bilateral profound sensorineural hearing loss (HL).[ncbi.nlm.nih.gov] Cardiac Anesthesia Heart Cardiac Catheterization Heart Cardiac Surgery Heart Cardiology Clinic Heart Cardiomyopathy Program Digestive Health Celiac Disease Psychologist Orthopedics[childrenscolorado.org] […] approaches for the treatment of microtia (a congenital ear deformity), Ms Rebecca Stockwell from The University of Queensland for her research into the spread of airborne diseases[medical-dictionary.thefreedictionary.com]

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