Literature DB >> 17473700

Cochlear implantation in Cockayne syndrome: our experience of two cases with different outcomes.

David P Morris1, Wael Alian, Heather Maessen, Cathy Creaser, Stephanie Demmons-O'Brien, Rene Van Wijhe, Manohar Bance.   

Abstract

Cockayne syndrome is a rare autosomal recessive defect in DNA repair resulting in a classic facies with potential visual and auditory impairment. The hearing loss begins peripherally and may become central as the condition progresses. Coexisting sensory deprivation from visual impairment and the possibility of progressive deterioration in mental function conspire with a lack of published experience to produce many challenges for the cochlear implant team. To the best of our knowledge, we present the first case reports with documented follow-up of cochlear implantation in two patients with different manifestations of Cockayne syndrome.

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Year:  2007        PMID: 17473700     DOI: 10.1097/MLG.0b013e3180325106

Source DB:  PubMed          Journal:  Laryngoscope        ISSN: 0023-852X            Impact factor:   3.325


  2 in total

Review 1.  Xeroderma pigmentosum-Cockayne syndrome complex.

Authors:  Valerie Natale; Hayley Raquer
Journal:  Orphanet J Rare Dis       Date:  2017-04-04       Impact factor: 4.123

2.  Bilateral cochlear implantation in a young patient with xeroderma pigmentosum (XP-D) and progressive sensorineural hearing loss-How to do it?

Authors:  H Woodun; H Woodun; R Vetrivel Vedachalam; H Fassihi; P Achar
Journal:  J Surg Case Rep       Date:  2022-01-14
  2 in total

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