22q13 deletion syndrome: an update and review for the primary pediatrician

Clin Pediatr (Phila). 2004 Jan-Feb;43(1):43-53. doi: 10.1177/000992280404300106.

Abstract

Recent advances in genetic testing can help to provide a specific diagnosis to children born with syndromes that result in congenital anomalies and developmental delay. One such emerging condition is the 22q13 deletion syndrome. With the introduction of subtelomeric fluorescence-in-situ hybridization (FISH) analysis, the 22q13 deletion has become recognized as a relatively widespread and underdiagnosed cause of mental retardation. Primary-care physicians play an important role in the care of children with 22q13 deletion syndrome, from suspecting the diagnosis in a developmentally delayed child through the medical, developmental, and behavioral aspects of their care. Furthermore, they serve as a valuable source of support and advocacy for the family and a resource for other care providers. The remainder of this article addresses the current state of knowledge regarding 22q13 deletion syndrome and offers the primary-care physician a framework in which to provide care and information.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.
  • Review

MeSH terms

  • Child
  • Chromosome Deletion
  • Chromosome Disorders / diagnosis*
  • Chromosome Disorders / genetics
  • Chromosome Disorders / therapy*
  • Chromosomes, Human, Pair 22*
  • Craniofacial Abnormalities / diagnosis
  • Craniofacial Abnormalities / genetics
  • Craniofacial Abnormalities / therapy
  • Developmental Disabilities / diagnosis*
  • Developmental Disabilities / genetics
  • Developmental Disabilities / therapy*
  • Humans
  • Primary Health Care*
  • Syndrome