Trisomy 21 Overview

Trisomy 21 Guide

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  • Summary
  • Definition
  • Symptoms
  • Causes
  • Treatment
  • Other Names
  • When to Contact a Medical Professional
  • Possible Complications
  • Outlook (Prognosis)
  • Prevention
  • Exams and Tests
  • Support Groups
  • References
Reviewed By Rachel A Lewis, MD

Definition

Down syndrome is a genetic condition in which a person has 47 chromosomes instead of the usual 46.


Symptoms

Down syndrome symptoms vary from person to person and can range from mild to severe. However, children with Down syndrome have a widely recognized characteristic appearance.

The head may be smaller than normal and abnormally shaped. For example, the head may be round with a flat area on the back. The inner corner of the eyes may be rounded instead of pointed.

Common physical signs include:


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Encyclopedia: Down Syndrome

Wikipedia.orgWIKIPEDIA.ORG

Down syndrome or trisomy 21 is a chromosomal disorder caused by the presence of all or part of an extra 21st chromosome. It is named after John Langdon Down, the British doctor who described the syndrome in 1866. The disorder was identified as a chromosome 21 trisomy by Jérôme Lejeune in 1959. The condition is characterized by a combination of major and minor differences in structure. Often Down syndrome is...


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Yahoo! Answers

Yahoo! AnswersYAHOO! ANSWERS

What are the 3 types of trisomy 21?
What are be the 3 types of trisomy 21 (Down Syndrome) and how are they...

the first poster had the types right. here are the causes of each Chromosome #21 can be damaged, for example, if one parent has two chromosomes at location 21, rather than...

Asked by Mike A - 9 months ago


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