A Study of Congenital and Early Acquired Impairment of Hearing

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dc.contributor.authorKalsotra, Parmod
dc.contributor.authorKumar, S
dc.contributor.authorGosh, P
dc.contributor.authorMishra, N K
dc.contributor.authorVerma, I C
dc.date.accessioned2016-01-25T12:05:35Z
dc.date.available2016-01-25T12:05:35Z
dc.date.issued2002-07
dc.description.abstractThe present study included 261 patients (M:F=I.72: I) suffering from congenital and early acquired hearing loss. The aetiological breakup of the hearing loss was: genetic factors 47.5%. non-genetic factors 16.8%, congenital ear malfonnations 8.5% and cryptogenic factors in 27.2% cases. Autosomal recessive mode of inheritance was seen most commonly (62%) followed by autosomal dominant (20%) in the genetic group of hearing loss. Maternal Rubella was most common cause of prenatal group of hearing loss while perinataly birth anoxia and prematurity were common. Postnataly meningitis was most common aetiology ofhearing loss. Linkage analysis on SLINK 2 point autosomal data yielded LOD score of more than 3 in an autosomal dominant family.en_US
dc.identifier.citationKalsotra Parmod, Kumar S, Gosh P, Mishra N K, Verma I C. A Study of Congenital and Early Acquired Impairment of Hearing. JK Science Journal of Medical Education and Research. 2002 Jul-Sept.4 (3): 138-143en_US
dc.identifier.urihttps://imsear.searo.who.int/handle/123456789/170919
dc.language.isoenen_US
dc.source.urihttps://www.jkscience.org/archive/Volume43/A%20studyof%20congenital%20and%20early.pdfen_US
dc.subjectCongenitalen_US
dc.subjectGeneticen_US
dc.subjectNon-geneticen_US
dc.subjectHearing lossen_US
dc.titleA Study of Congenital and Early Acquired Impairment of Hearingen_US
dc.typeArticleen_US
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