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19 Possible Causes for Bilateral Congenital Profound Sensorineural Hearing Loss, Torsades De Pointes

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  • 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] de pointes (TdP) VT.[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] Get Update Overview Congenital long QT syndrome is electrocardiographically characterized by a prolonged QT interval and polymorphic ventricular arrhythmias (torsade de pointes[diseaseinfosearch.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] ECG criteria for torsade de pointes Prolonged QTc interval before appearance of torsade de pointes.[ecgwaves.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] Cardiac arrest or fainting due to trademark cardiac arrhythmia called torsade de pointes Family history – of a SADS diagnosis, SADS symptoms, or sudden unexplained death of[sads.org] However, if a torsades de pointes episode lasts longer, it can result in a sudden fainting spell followed by a full-body seizure.[mayoclinic.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] ECG criteria for torsade de pointes Prolonged QTc interval before appearance of torsade de pointes.[ecgwaves.com] de pointes Torsades type ventricular tachycardia Clinical Information A condition that is characterized by episodes of fainting (syncope) and varying degree of ventricular[icd10data.com]

  • Jervell-Lange-Nielsen Syndrome Type 2

    The second symptom is a congenital bilateral profound sensorineural hearing loss.[hearinghealthmatters.org] The proband had long QTc, bilateral high-tone sensorineural deafness, recurrent syncope, and Torsades de Pointes.[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]

  • Congenital Deafness

    hearing loss ranges from mild to profound hearing loss.[wvdhhr.org] There is prolongation of the QT interval, torsade de pointe arrhythmias (turning of the points, in reference to the apparent alternating positive and negative QRS complexes[dizziness-and-balance.com] In syndromic hearing loss, the auditory pathology may be conductive and/or sensorineural, unilateral or bilateral, symmetrical or asymmetrical, and progressive or stable.[wvdhhr.org]

  • 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] Patient with LQTS may present with syncope, seizures or sudden cardiac death secondary to polymorphic ventricular tachycardia (VT) or torsades de pointes.[ijaweb.org] de pointes and sudden cardiac death.[en.wikipedia.org]

  • Tricho-Retino-Dento-Digital Syndrome

    Symptoms INHERITANCE: Autosomal recessive HEAD AND NECK: [Ears]; Bilateral congenital profound sensorineural hearing loss; [Mouth]; Diastema; [Teeth]; Oligodontia Ehlers-Danlos[findzebra.com] de pointes Torsion dystonia 7 Torticollis Torticollis keloids cryptorchidism renal dysplasia Torulopsis Tosti–Misciali–Barbareschi syndrome Total hypotrichosis, Mari type[ipfs.io] […] maladie Toni–Fanconi syndrome TORCH syndrome Toriello–Carey syndrome Toriello–Lacassie–Droste syndrome Toriello syndrome Toriello–Higgins–Miller syndrome Torres–Ayber syndrome Torsades[ipfs.io]

  • 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] Atrial septal defect 7 with or without atrioventricular conduction defects Torsades de pointes A type of ventricular tachycardia characterized by polymorphioc QRS complexes[amp.pharm.mssm.edu]

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