Chapter

Rare Diseases Epidemiology

Volume 686 of the series Advances in Experimental Medicine and Biology pp 433-453

Date:

The Contribution of Rare Diseases to Understanding the Epidemiology of Neurodevelopmental Disabilities

  • Diana SchendelAffiliated withNational Center on Birth Defects and Developmental Disabilities, Centers for Disease Control and Prevention Email author 
  • , Catherine RiceAffiliated withNational Center on Birth Defects and Developmental Disabilities, Centers for Disease Control and Prevention
  • , Christopher CunniffAffiliated withDepartment of Pediatrics, University of Arizona College of Medicine

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Abstract

Our objective is to describe the contribution of rare diseases to our understanding of the epidemiology of neurodevelopmental disabilities (NDDs) by comparing and contrasting the epidemiologic features of NDDs classified according to key characteristics of developmental delay or deviance in such areas as behavior or cognition (the phenotypic approach; autism spectrum disorders and intellectual disability as examples) versus classification based on the identification of an etiologic diagnosis (the etiologic approach; 22q11.2 deletion syndrome and fragile X syndrome as examples). We suggest specific applications in which consideration of rare etiology-based NDDs might further our understanding of NDD epidemiology overall; what is needed to integrate the two classification approaches; and identify practical challenges in achieving that integration. Understanding commonalities and differences in the epidemiologic features of the phenotypically and etiologically defined NDD classifications provides a useful framework for furthering our understanding of the prevalence, distribution, and causes of NDDs, as well as delivering appropriate diagnostic resources, appropriate treatments, accurate prognostic information, and estimates of recurrence risk for these disorders.

Keywords

Neurodevelopmental disabilities Rare disorders Epidemiology Autism spectrum disorders Intellectual disability Fragile X syndrome 22q11.2 deletion syndrome