Skip Navigation LinksHome > February 2009 - Volume 9 - Issue 1 > A Parent's Guide to the Genetics of Down Syndrome
Advances in Neonatal Care:
doi: 10.1097/01.ANC.0000346092.50981.c0
The Long Road Home

A Parent's Guide to the Genetics of Down Syndrome

Hartway, Sarah MS, RN

Section Editor(s): FORSYTHE, PAULA MSN, CNS

Collapse Box

Abstract

Down syndrome is a genetic disorder, occurring when an individual has all or part of an extra copy of chromosome 21. Parents of children with Down syndrome are often confused by the term genetic disorder because they associate the term with inheritance but have also learned that Down syndrome is not typically inherited. These parents may have questions about the nature of chromosomes, how Down syndrome occurs, recurrence risk and more. This article attempts to address many of the common questions parents of children with Down syndrome express regarding the genetics of the disorder including the mechanisms by which Down syndrome occurs: nondisjunction, translocation and mosaicism, as well as providing information about prenatal testing options, how the diagnosis is made and where parents may go for further information.

© 2009 National Association of Neonatal Nurses

Login

Search for Similar Articles
You may search for similar articles that contain these same keywords or you may modify the keyword list to augment your search.