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57 Possible Causes for Bilateral Congenital Profound Sensorineural Hearing Loss, Hearing Problem, Retinitis Pigmentosa

  • Congenital Deafness

    LXXIX The Association of Nerve Deafness and Retinitis Pigmentosa Interval Report . Annals of Otology, Rhinology & Laryngology, Vol. 69, Issue. 4, p. 1044.[journals.cambridge.org] Infant/Toddler Hearing Checklist Parents are often the first people to sense that their child has a hearing problem.[pamf.org] hearing loss ranges from mild to profound hearing loss.[wvdhhr.org]

  • AMACR Deficiency

    […] loss, diabetes mellitus, mental problems, and hypogonadism.[ncbi.nlm.nih.gov] , bilateral, profound sensorineural hearing loss, vestibular areflexia, and adolescent-onset retinitis pigmentosa.[refsumdisease.org] Retinal changes have been reported in five patients and vary from retinal pigmentary epithelial changes to retinitis pigmentosa [7, 9, 11, 12, 14].[ojrd.biomedcentral.com]

  • Usher Syndrome Type 1

    In view of the combination of profound hearing loss, vestibular dysfunction, and retinitis pigmentosa in the patients, we classified the disease as USH1.[ncbi.nlm.nih.gov] Typically, students develop notable hearing problems by adolescence.[sess.ie] , profound sensorineural hearing loss, adolescent-onset retinitis pigmentosa and loss of vestibular function.[ltd.aruplab.com]

  • Usher Syndrome Type 1J

    All newborn babies are screened for hearing problems. If a hearing problem is found in the newborn, the baby will have follow-up testing.[hopkinsmedicine.org] 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] Duane retraction syndrome has earlier been reported with various conditions such as retinitis pigmentosa, Bardet Biedl syndrome with atypical retinitis pigmentosa, pseudoretinitis[healio.com]

  • Usher Syndrome Type 1H

    These types are distinguished by the severity of hearing loss, the presence or absence of balance problems, and the age at which signs and symptoms appear.[ncbi.nlm.nih.gov] Usher syndrome type I is characterized by congenital, bilateral, profound sensorineural hearing loss, vestibular areflexia, and adolescent-onset retinitis pigmentosa.[ncbi.nlm.nih.gov] Degeneration of these sensory cells causes the hearing loss, balance problems, and vision loss that occur with Usher syndrome .[ghr.nlm.nih.gov]

  • Deafness

    Websites Table Of Contents External Websites How Stuff Works - Healthguide - Hearing Loss and Deafness British Broadcasting Corporation - Deafness and Hearing Problems National[web.archive.org] 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] Further, none of the affected patients showed any associated symptoms, such as hypertrophic cardiomyopathy or retinitis pigmentosa.[ncbi.nlm.nih.gov]

  • Usher Syndrome Type 1K

    These types are distinguished by the severity of hearing loss, the presence or absence of balance problems, and the age at which signs and symptoms appear.[ncbi.nlm.nih.gov] Usher syndrome type I is characterized by congenital, bilateral, profound sensorineural hearing loss, vestibular areflexia, and adolescent-onset retinitis pigmentosa.[ncbi.nlm.nih.gov] 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]

  • Refsum Disease

    Symptoms of IRD begin in infancy with a visual impairment called retinitis pigmentosa, which often leads to blindness, and hearing problems that usually progress to deafness[sharecare.com] 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] Refsum disease is a potentially lethal and disabling condition associated with retinitis pigmentosa in which early treatment can prevent some of the systemic manifestations[ncbi.nlm.nih.gov]

  • Usher Syndrome Type 1D

    Hearing problems are noticed by the teenage years and they become deaf by mid-to-late adulthood. Night blindness starts around puberty.[patient.info] Usher syndrome type I is characterized by congenital, bilateral, profound sensorineural hearing loss, vestibular areflexia, and adolescent-onset retinitis pigmentosa.[ncbi.nlm.nih.gov] Usher syndrome - sensorineural hearing loss and retinitis pigmentosa.[medical-dictionary.thefreedictionary.com]

  • Usher Syndrome Type 3B

    Hearing problems are noticed by the teenage years and they become deaf by mid-to-late adulthood. Night blindness starts around puberty.[patient.info] 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] USH is a genetically heterogeneous condition characterized by the association of retinitis pigmentosa with sensorineural deafness.[uniprot.org]

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