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Trisomy 3 mosaicism

Trisomy 3 mosaicism: Introduction

Trisomy 3 mosaicism: A very rare chromosomal disorder where there is an extra copy of chromosome 3 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. More detailed information about the symptoms, causes, and treatments of Trisomy 3 mosaicism is available below.

Symptoms of Trisomy 3 mosaicism

Home Diagnostic Testing

Home medical testing related to Trisomy 3 mosaicism:

Causes of Trisomy 3 mosaicism

Read more about causes of Trisomy 3 mosaicism.

Trisomy 3 mosaicism: Research Doctors & Specialists

Research related physicians and medical specialists:

Other doctor, physician and specialist research services:

Hospitals & Clinics: Trisomy 3 mosaicism

Research quality ratings and patient safety measures for medical facilities in specialties related to Trisomy 3 mosaicism:

Choosing the Best Hospital: More general information, not necessarily in relation to Trisomy 3 mosaicism, on hospital performance and surgical care quality:

Statistics for Trisomy 3 mosaicism

Trisomy 3 mosaicism: Broader Related Topics

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Definitions of Trisomy 3 mosaicism:

Ophanet, a consortium of European partners, currently defines a condition rare when it affects 1 person per 2,000. They list Trisomy 3 mosaicism as a "rare disease".
Source - Orphanet

Related Trisomy 3 mosaicism Info

Videos about Trisomy 3 mosaicism

 

More information about Trisomy 3 mosaicism

  1. Trisomy 3 mosaicism: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Home Testing
 

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