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Genetic Testing in Pregnancy 

Introduction

1. The Triple Test - Overview

2. The Triple Test - Detail and Results

3. Amniocentesis

4. CVS

 

 

During pregnancy, there are some medical procedures that are available to parents that allow them to test whether or not certain genetic disorders are

present in their child.  In some countries, certain tests are obligatory whilst others are only available under very strict circumstances. In others countries the three main tests are all entirely voluntary, whilst in some countries the tests are not available at all.  You will need to ask your medical practitioner which tests are available and which are compulsory in your own location.

 

The Ethics of Choice:

Some parents object to any or some forms of genetic disorder testing.  This can be for a variety of reasons:

NOTE:  In the second point above (anti-abortion stance), it should be noted that many people who discover that they have a child with a genetic disorder (such as Down Syndrome) often decide to continue with the pregnancy.   The fact that they discovered the information early on in the pregnancy allows them to prepare for the lifestyle changes that inevitably follow by collecting information and contacting support groups in their area which can be of great assistance under these circumstances.

 

This article explains the following test procedures; 'The Triple Test' (also known as 'AFP Plus' or 'Multiple Marker Screening'), Amniocentesis and CVS (Chorionic Villus Sampling)

 

Part 2 of this article Genetic Disorders continues the subject with a look at several genetic disorders that can manifest themselves, many of which can be discovered by use of the tests described here.

 

Introduction

1. The Triple Test - Overview

2. The Triple Test - Detail and Results

3. Amniocentesis

4. CVS

 

 

 

 

 

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