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Trisomy 12 mosaicism

Trisomy 12 mosaicism: Introduction

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. More detailed information about the symptoms, causes, and treatments of Trisomy 12 mosaicism is available below.

Symptoms of Trisomy 12 mosaicism

Home Diagnostic Testing

Home medical testing related to Trisomy 12 mosaicism:

Causes of Trisomy 12 mosaicism

Read more about causes of Trisomy 12 mosaicism.

Trisomy 12 mosaicism: Research Doctors & Specialists

Research related physicians and medical specialists:

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Hospitals & Clinics: Trisomy 12 mosaicism

Research quality ratings and patient safety measures for medical facilities in specialties related to Trisomy 12 mosaicism:

Choosing the Best Hospital: More general information, not necessarily in relation to Trisomy 12 mosaicism, on hospital performance and surgical care quality:

Statistics for Trisomy 12 mosaicism

Trisomy 12 mosaicism: Broader Related Topics

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Definitions of Trisomy 12 mosaicism:

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

Related Trisomy 12 mosaicism Info

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More information about Trisomy 12 mosaicism

  1. Trisomy 12 mosaicism: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Home Testing
 

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