Array-CGH analysis in Rwandan patients presenting development delay/intellectual disability with multiple congenital anomalies

BMC Med Genet. 2014 Jul 12:15:79. doi: 10.1186/1471-2350-15-79.

Abstract

Background: Array-CGH is considered as the first-tier investigation used to identify copy number variations. Right now, there is no available data about the genetic etiology of patients with development delay/intellectual disability and congenital malformation in East Africa.

Methods: Array comparative genomic hybridization was performed in 50 Rwandan patients with development delay/intellectual disability and multiple congenital abnormalities, using the Agilent's 180 K microarray platform.

Results: Fourteen patients (28%) had a global development delay whereas 36 (72%) patients presented intellectual disability. All patients presented multiple congenital abnormalities. Clinically significant copy number variations were found in 13 patients (26%). Size of CNVs ranged from 0,9 Mb to 34 Mb. Six patients had CNVs associated with known syndromes, whereas 7 patients presented rare genomic imbalances.

Conclusion: This study showed that CNVs are present in African population and show the importance to implement genetic testing in East-African countries.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Abnormalities, Multiple / genetics*
  • Adolescent
  • Child
  • Child, Preschool
  • Comparative Genomic Hybridization / methods*
  • DNA Copy Number Variations
  • Developmental Disabilities / genetics*
  • Female
  • Genetic Variation
  • Humans
  • Intellectual Disability / genetics*
  • Male
  • Rwanda