Deletion of 8p: a report of a child with normal intelligence

Gilmore, L., Cuskelly, M., Jobling, A. and Smith, S. (2001) Deletion of 8p: a report of a child with normal intelligence. Developmental Medicine And Child Neurology, 43 12: 843-846. doi:10.1017/S0012162201001530


Author Gilmore, L.
Cuskelly, M.
Jobling, A.
Smith, S.
Title Deletion of 8p: a report of a child with normal intelligence
Journal name Developmental Medicine And Child Neurology   Check publisher's open access policy
ISSN 0012-1622
Publication date 2001-01-01
Sub-type Article (original research)
DOI 10.1017/S0012162201001530
Volume 43
Issue 12
Start page 843
End page 846
Total pages 4
Editor M. C. O. Bax
Place of publication Cambridge
Publisher Cambridge University Press
Language eng
Subject C1
380106 Developmental Psychology and Ageing
750305 Ability and disability
Abstract The case is presented of a female infant with a distal deletion of 8p (8p23.1 --> pter) whose development was monitored over a 5-year period from 12 months of age. Although previous literature has suggested that 8p deletion is associated with mild to moderate intellectual disability, the child reported here has normal intelligence. Despite initial delays in gross motor and language skills, cognitive development (assessed with the Bayley Scales of Infant Development) and intellectual ability (measured on the Stanford-Binet Intelligence Scale) were within average range. It is argued that the small number of previous case reports may have created a misleading impression of intellectual development in individuals with distal deletions of 8p.
Keyword Clinical Neurology
Pediatrics
Distal 8p
Mental-retardation
Terminal Deletion
8p23.1
Deficiency
Phenotype
Features
Q-Index Code C1

Document type: Journal Article
Sub-type: Article (original research)
Collection: School of Education Publications
 
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Created: Wed, 15 Aug 2007, 02:03:12 EST