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  • DD of Hearing Loss

    Загружено:

    Nitin Sharma
    9 просмотров1 страница
    This document provides a differential diagnosis for non-organic hearing loss categorized into sensorineural hearing loss, conductive hearing loss, and sensorineural hearing loss due to genetic syndromes and non-syndromic causes. Specific acquired and infectious etiologies are listed under sensorineural hearing loss. Conductive hearing loss can be caused by issues with the external auditory canal, tympanic membrane, or middle ear space. Genetic causes of sensorineural hearing loss include syndromic and non-syndromic forms that are autosomal recessive, autosomal dominant, or X-linked.

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    DD OF HEARING LOSS

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    This document provides a differential diagnosis for non-organic hearing loss categorized into sensorineural hearing loss, conductive hearing loss, and sensorineural hearing loss due to genetic syndromes and non-syndromic causes. Specific acquired and infectious etiologies are listed under sensorineural hearing loss. Conductive hearing loss can be caused by issues with the external auditory canal, tympanic membrane, or middle ear space. Genetic causes of sensorineural hearing loss include syndromic and non-syndromic forms that are autosomal recessive, autosomal dominant, or X-linked.

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    Attribution Non-Commercial (BY-NC)
    Скачайте в формате PDF, TXT или читайте онлайн в Scribd
    Отметить как неприемлемый контент
    9 просмотров1 страница

    DD of Hearing Loss

    Загружено:

    Nitin Sharma
    This document provides a differential diagnosis for non-organic hearing loss categorized into sensorineural hearing loss, conductive hearing loss, and sensorineural hearing loss due to genetic syndromes and non-syndromic causes. Specific acquired and infectious etiologies are listed under sensorineural hearing loss. Conductive hearing loss can be caused by issues with the external auditory canal, tympanic membrane, or middle ear space. Genetic causes of sensorineural hearing loss include syndromic and non-syndromic forms that are autosomal recessive, autosomal dominant, or X-linked.

    Авторское право:

    Attribution Non-Commercial (BY-NC)
    Скачайте в формате PDF, TXT или читайте онлайн в Scribd
    Отметить как неприемлемый контент
    из 1

    Table 1.

    Non-Organic Hearing Loss

    Differential diagnosis of hearing loss.


    Sensorineural Hearing Loss Acquired Toxins Aminoglycosides Platins Erythromycin Loop diuretics Quinines Salicylates Infectious CMV EBV Herpes simplex virus HIV Meningitis Mumps Rubella Syphilis Other Noise Trauma Perilymph fistula Hyperbilirubinemia Multiple sclerosis Endolymphatic hydrops Michel aplasia Labyrinthitis obliterans Conductive Hearing Loss External auditory canal Cerumen impaction Atresia Stenosis

    Sensorineural Hearing Loss Genetic Syndromic Alport Branchio-oto-renal Jervell and Lange Nielsen Neurofibromatosis II Norrie disease Pendred Stickler Treacher-Collins Usher Waardenburg Non-syndromic Autosomal-recessive Loci DFNB 1-30 Autosomal dominant Loci DFNA 1-39 X-Linked Loci DFN 1-6 Mitochondrial

    Hearing Loss and Balance Disorders

    Tympanic Membrane (TM) TM retraction Tympanosclerosis TM perforation TM atalectasis Middle Ear Space Otitis media with effusion Cholesteatoma Glomus High-riding jugular bulb Dehiscent carotid artery Perilymphatic fistula Other masses Ossicles Discontinuity Atresia of the oval window Displaced Persistent stapedial artery Agenesis

    63

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