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Neurocognitive functioning of a child with partial trisomy 6 and monosomy 21.

Abstract
This case study describes the neurocognitive presentation of a child with identified genetic abnormalities of trisomy 6 and monosomy 21 who was evaluated as part of a standard medical protocol for cochlear implantation following diagnosis of profound sensorineural hearing loss. This child received neurocognitive testing prior to cochlear implantation and approximately 12 months post-activation of his cochlear implant. While he has not fully developed oral language, his presentation suggested improvement in overall skills since the activation of the cochlear implant; however, less than would be expected for a typically developing child.
AuthorsJennifer M Katzenstein, John S Oghalai, Ross Tonini, Dian Baker, Jody Haymond, Susan E Caudle
JournalNeurocase (Neurocase) Vol. 15 Issue 2 Pg. 97-100 ( 2009) ISSN: 1465-3656 [Electronic] England
PMID19172430 (Publication Type: Case Reports, Journal Article)
Topics
  • Child Development (physiology)
  • Child, Preschool
  • Chromosomes, Human, Pair 21
  • Chromosomes, Human, Pair 6
  • Cochlear Implants
  • Cognition (physiology)
  • Cognition Disorders (physiopathology)
  • Humans
  • Male
  • Monosomy (physiopathology)
  • Neuropsychological Tests
  • Severity of Illness Index
  • Trisomy (physiopathology)

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