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What is Trisomy 12 mosaicism?

What is Trisomy 12 mosaicism?

  • Trisomy 12 mosaicism: A very rare chromosomal disorder where there is an extra copy of chromosome 12 in some of the body's cells. Some cases with this chromosomal abnormality have no clinical symptoms. The presence of abnormalities in some cases is dependent on which body cells contain the chromosomal defect.

Ophanet, a consortium of European partners, currently defines a condition rare when it affects 1 person per 2,000. They list Trisomy 12 mosaicism as a "rare disease".
Source - Orphanet

Trisomy 12 mosaicism: Introduction

Types of Trisomy 12 mosaicism:

Broader types of Trisomy 12 mosaicism:

What causes Trisomy 12 mosaicism?

Causes of Trisomy 12 mosaicism: see causes of Trisomy 12 mosaicism

What are the symptoms of Trisomy 12 mosaicism?

Symptoms of Trisomy 12 mosaicism: see symptoms of Trisomy 12 mosaicism

Trisomy 12 mosaicism: Testing

Diagnostic testing: see tests for Trisomy 12 mosaicism.

How is it treated?

Doctors and Medical Specialists for Trisomy 12 mosaicism: Medical Geneticist ; see also doctors and medical specialists for Trisomy 12 mosaicism.
Treatments for Trisomy 12 mosaicism: see treatments for Trisomy 12 mosaicism

Name of Trisomy 12 mosaicism

Main name of condition: Trisomy 12 mosaicism

 

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