Pediatric Neurology
Volume 41, Issue 6 , Pages 391-398, December 2009

Chromosomal Microarray Interpretation: What Is a Child Neurologist to Do?

  • Alex R. Paciorkowski, MD

      Affiliations

    • Division of Pediatric and Developmental Neurology, Department of Neurology, Washington University School of Medicine, St. Louis, Missouri
    • Corresponding Author InformationCommunications should be addressed to: Dr. Paciorkowski; Division of Pediatric and Developmental Neurology; Department of Neurology; Washington University School of Medicine; Campus Box 8111; 660 South Euclid Avenue; St. Louis, MO 63110-1093.
  • ,
  • Min Fang, MD, PhD

      Affiliations

    • Clinical Research Division, Department of Pathology, Fred Hutchinson Cancer Research Center, University of Washington, Seattle, Washington

Received 25 February 2009; accepted 4 May 2009.

The chromosomal microarray now plays a central role in the evaluation of children with neurologic developmental disorders, including global developmental delay, mental retardation, and increasingly also autistic spectrum disorders. As arrays become more sophisticated and their use more widespread, the child neurologist is likely to encounter abnormal chromosomal microarray results. The interpretation of such data is not always straightforward. This review article discusses in a practical manner the nature of chromosomal microarray results, describes an algorithm to help the child neurologist navigate a variety of testing scenarios, and proposes a standardized system for ranking array data based on levels of evidence of genotype-phenotype correlation.

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PII: S0887-8994(09)00268-9

doi:10.1016/j.pediatrneurol.2009.05.003

Pediatric Neurology
Volume 41, Issue 6 , Pages 391-398, December 2009