High Risk Indicators associated with Childhood hearing loss
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| High Risk factors associated with | permanent congenital, delayed-onset, or progressive hearing loss in childhood
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| 1 | caregiver concerns regarding hearing, speech, language or developmental delay
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| 2 | family history of permanent childhood hearing loss
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| 3 | neonatal intensive care for more than 5 days or any of the following: ECMO, assisted venitlation, exposure to ototoxic medications or loop diuretics and hyperbilirubinemia
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| 4 | in utero infections such as CMV, herpes, rubella, syphilis, and toxoplasmosis
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| 5 | craniofacial anomalies, including those that involved the pinna, ear canal, ear tags, ear pits, and temporal bone anomalies
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| 6 | physical findings, such as a white forelock, that are associated with a syndrome known to include a sensorineural or permanent conductive hearing loss
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| 7 | syndromes associated with hearing loss: e.g. neurofibromatosis, osteopetrosis, Usher syndrome; also Waardenburg, Alport, Pendred, Jervell and Lange and Nielson
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| 8 | neurodegenerative disorders such as Hunter syndrome, or sensory motor neuropathies, such as Friedreich ataxia and Charcot-Marie-Tooth syndrome
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| 9 | culture-positive postnatal infections associated with sensorineural hearing loss, including confirmed bacterial and viral meningitis
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| 10 | head trauma, especially basal skull/temporal bone fracture that requires hospitalization
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| 11 | chemotherapy
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