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Rudolph's PediatricsRudolph's Pediatrics

Section 19. Disorders of the Ear, Nose, and Throat > 

Chapter 369. The Ear

Disorders of the Ear

John H. Greinwald Jr., Margaret A. Kenna, and Blake C. Papsin
Topics Discussed: adverse effects caused by therapeutic use of aminoglycosides; aspirin toxicity; barotrauma; bone anchored hearing aid; cholesteatoma; chondritis; cisplatin; cochlear implantation; cochlear implants; congenital deafness; cytomegalovirus; cytomegalovirus infection; dizziness; ear; ear diseases; ear neoplasms; ear, external; ear, middle; ear, nose, and throat; exostoses; frostbite; furosemide; hearing aids; hearing impairment; hearing loss, conductive; hearing loss, inherited; injury of ear; inner ear; isotretinoin; labyrinthine fistula; labyrinthitis; labyrinthitis, bacterial; middle ear mass; osteochondroma; osteoma; otitis externa; otitis media; ototoxicity; perichondritis; salicylate toxicity; sensorineural hearing loss; torch syndrome; tympanic membrane perforation; vertigo.
Sections: References.
Excerpt:"Approximately 1 in 1500 children has a severe to profound hearing loss at birth or in early childhood. This relatively high incidence, the high likelihood of significant negative developmental impact in children with hearing loss, and the significant technological capabilities to habilitate children with hearing loss have lead to most developed countries instituting universal newborn hearing screening protocols. These protocols are designed to identify all children with hearing loss at an early age so that intervention can be provided during the critical early periods of speech and language development.5,6The most common causes of acquired hearing loss in children is a conductive hearing loss that results from abnormalities of the middle ear (especially otitis media and ossicular abnormalities), whereas congenital hearing loss is often a result of sensorineural deficits. The most likely congenital etiology is the embryologic retention of an epithelial cell rest in the middle ear space. Acquired cholesteatomas may occur as the result of perforation or severe tympanic membrane retraction. Rarely, they can occur at the site of a tympanostomy tube insertion. Chronic negative middle ear pressure may cause a segment of weakened tympanic membrane to retract either in the attic region or in the posterior-superior quadrant. These retractions can cause the inhibition of the natural epithelial migration of desquamated squamous debris. Debris may become wet and infected, producing foul-smelling..."
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