@article {Bathla:2013:2637-8329:144,
title = "Imaging of Congenital and Acquired Sensorineural Hearing loss: Peeking through the Oval Window into the Cochlea and Beyond",
journal = "Neurographics",
parent_itemid = "infobike://asnr/ng",
publishercode ="asnr",
year = "2013",
volume = "3",
number = "3",
publication date ="2013-09-01T00:00:00",
pages = "144-154",
itemtype = "ARTICLE",
issn = "2637-8329",
eissn = "2637-8329",
url = "https://asnr.publisher.ingentaconnect.com/content/asnr/ng/2013/00000003/00000003/art00005",
doi = "doi:10.3174/ng.3130062",
keyword = "GRE = gradient recalled echo, IAC = internal auditory canal, GA = gestational age, EVAS = enlarged vestibular aqueduct syndrome, SNHL = sensorineural hearing loss, CPA = cerebellopontine angle, CHARGE = Coloboma, Heart defect, Atresia choanae, Retarded growth and development, Genital hypoplasia, Ear anomalies/deafness, ELST = endolymphatic sac tumor, CND = cochlear nerve deficiency, CN = cranial nerve, CMV = Cytomegalovirus, SCC = semicircular canal",
author = "Bathla, G. and Smoker, W.R.K.",
abstract = "Pure sensorineural hearing loss may be congenital or acquired. It can result from a constellation of abnormalities that may involve the labyrinth, internal auditory canal, CPA, brain stem, or auditory pathways. CT and MR imaging often play a complementary role in its evaluation and
postoperative assessment and in ascertaining overall prognosis. Herein we review the spectrum of pathology along the auditory pathway, extending from the labyrinth to the auditory cortex, that may present with sensorineural hearing.Learning Objective: To recognize the imaging spectrum
of sensorineural hearing loss in the pediatric and adult population.",
}