Literature DB >> 12815515

Interstitial deletion on chromosome 5q33.3q35.1 in a 6-year-old girl -- neuropsychological findings and follow-up in an extremely rare chromosomal aberration.

Dietmar Heubrock1, Stephanie Spranger, Bergit Lex, Anja C Lepach, Franz Petermann.   

Abstract

Interstitial deletion on chromosome 5q33.3q35.1 is an extremely rare chromosomal aberration for which a characteristic syndrome could not yet be delineated. In most patients with 5q deletions severe mental retardation is described. Recently, Spranger et al. (2000) described the case of a 4-year-old girl with a de novo deletion on 5q33.3q35.1 presenting only with mild psychomotor delay, minor facial anomalies, and seizures. The patient was admitted for outpatient neuropsychological assessment when she was 6.2 years old. Neurocognitive tests revealed an overall developmental delay of about 32 months and an intelligence score in the range of mild mental retardation. Her cognitive phenotype was characterized by a considerable visual-spatial deficit in the form of disorganized drawings or block designs indicating a profound lack of cohesion and overall global organization (decay of gestalt). The patient's behavioral phenotype was dominated by a distinct disinhibition syndrome demonstrating severe hyperactivity, utilization behavior, and aggressive behavior.

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Year:  2003        PMID: 12815515     DOI: 10.1076/chin.9.2.129.14502

Source DB:  PubMed          Journal:  Child Neuropsychol        ISSN: 0929-7049            Impact factor:   2.500


  1 in total

1.  Interstitial deletion of 5q33.3q35.1 in a boy with severe mental retardation.

Authors:  Jin Hwan Lee; Hyo Jeong Kim; Jung Min Yoon; Eun Jung Cheon; Jae Woo Lim; Kyong Og Ko; Gyung Min Lee
Journal:  Korean J Pediatr       Date:  2016-11-30
  1 in total

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