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60 Possible Causes for Bilateral Congenital Profound Sensorineural Hearing Loss, Pediatric Disorder

  • Usher Syndrome Type 1

    , profound sensorineural hearing loss, adolescent-onset retinitis pigmentosa and loss of vestibular function.[ltd.aruplab.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] Clinical diagnosis for type 1 is based on findings of bilateral sensorineural hearing loss symmetric, congenital and profound.[cags.org.ae]

  • Congenital Cytomegalovirus Infection

    One child with profound sensorineural hearing loss had severe bilateral temporal bone dysplasia with a small cochlea lacking an interscalar septum, an abnormal vestibule,[ncbi.nlm.nih.gov] Track 4-1 Hemoglobinopathies Track 4-2 Hemophilia and Idiopathic Thrombocytopenic Track 4-3 Pediatric Bleeding Disorders Track 4-4 Lymphoma and Leukemia Track 4-5 Blood Transfusion[pediatrics.euroscicon.com] Semin Pediatr Infect Dis . 2005;16:44–49. doi:10.1053/j.spid.2004.09.011 [CrossRef] Bale JF Jr, . Human cytomegalovirus infection and disorders of the nervous system.[healio.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] The Arthritis Foundation The American Academy of Pediatrics[webmd.com] Hearing loss is always bilateral, congenital, sensorineural and profound. Psychomotor development is normal.[orpha.net]

  • Refsum Disease

    Daniel Hohl and Mary Williams, Mendelian Disorders of Cornification (MEDOC): The Ichthyoses, Harper's Textbook of Pediatric Dermatology, (121.1-121.70), (2011).[doi.org] Retinitis pigmentosa and sensorineural hearing loss Usher syndrome type I is characterized by a congenital, bilateral, profound sensorineural deafness, vestibular areflexia[ncbi.nlm.nih.gov] Retinitis pigmentosa and sensorineural hearing loss Usher syndrome type I is characterized by a congenital , bilateral, profound sensorineural deafness, vestibular areflexia[ncbi.nlm.nih.gov]

  • Glutamate Formiminotransferase Deficiency

    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] […] hematologic disorders, including newly recognized ones.[books.google.com] Pediatric Research 14(4, II): 537, 1980 Folic acid deficiency in congenital disorders.[eurekamag.com]

  • 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] Pediatrics 35 : Celes-Blaubach A, Garcia-Zozaya J, Perez-Requejo J, Brass K. (1974). Vestibular disorders in Alport's syndrome.[docplayer.net] 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]

  • Microtia

    […] canals, and bilateral profound sensorineural hearing loss (HL).[ncbi.nlm.nih.gov] […] voice and airway disorders including respiratory papillomatosis and subglottic stenosis pediatric sinus disease advanced surgery for obstructive sleep apnea facial nerve[floatinghospital.org] Balance and Vestibular Disorders Clinic Digestive Health Pediatric Endoscopy Surgery Pediatric General Surgery Digestive Health Pediatric Liver Center Pharmacy Services Surgery[childrenscolorado.org]

  • Congenital Deafness

    hearing loss ranges from mild to profound hearing loss.[wvdhhr.org] Pediatr Blood Cancer, 58(2): 314-5 [ CR ] [ PM ] [ EČ ][ GS ] Singh, N., Nainani, N., Arora, P., Venuto, R.C. (2009) CKD in MYH9-related disorders.[scindeks.ceon.rs] Vick, assistant professor of psychological sciences, biomedical engineering and pediatrics, for her work titled “Treatment for Severe Speech Disorders in Children: Identifying[thedaily.case.edu]

  • 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] , Jeddah, Kingdom of Saudi Arabia. 4 Department of Pediatric Cardiology, Emma Children's Hospital, Academic Medical Centre, Amsterdam, The Netherlands; Department of Pediatric[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]

  • Deafness

    Mumps (Epidemic parotitis) may result in profound sensorineural hearing loss (90 dB or more), unilateral (one ear) or bilateral (both ears). congenital rubella (also called[en.wikipedia.org] With regards to pediatric patients, severe hearing impairment or deafness affects about 1 in 1,000 neonates and usually results from genetic disorders or intrauterine infections[symptoma.com] Pediatrics 2001;108:40–43. National Institute on Deafness and Other Communication Disorders. Quick Statistics. Bethesda, MD: U.S.[web.archive.org]

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