[Phenotypic and genetic analysis of a child featuring multiple malformations due to copy number variation on chromosome 5]

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2014 Feb;31(1):56-9. doi: 10.3760/cma.j.issn.1003-9406.2014.01.013.
[Article in Chinese]

Abstract

Objective: To determine the origin of chromosomal aberration for a child featuring multiple malformation, and to correlate the genotype with phenotype.

Methods: Routine G-banding was performed to analyze the karyotype of the patient and her parents, and array comparative genomic hybridization (array CGH) was used for fine mapping of the aberrant region.

Results: The karyotype of the child was ascertained as 46,XY. Array CGH has mapped a 14.21 Mb deletion to 5p15.2p15.33, and a very small 3.67 Mb duplication to 5q35.3. The patient has presented features such as mental retardation, heart defect, low-set ears, hypertelorism and down-slanting palpebral fissures.

Conclusion: Chromosome 5 copy number variation can cause multiple malformation. In contrast to routine karyotype analysis, array CGH can map aberrant region with much higher resolution and accuracy.

Publication types

  • English Abstract

MeSH terms

  • Abnormalities, Multiple / diagnosis
  • Abnormalities, Multiple / genetics*
  • Chromosome Aberrations*
  • Chromosomes, Human, Pair 5*
  • DNA Copy Number Variations*
  • Genotype
  • Humans
  • Infant
  • Male
  • Phenotype