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Chromosome 22, trisomy

Chromosome 22, trisomy: Introduction

Chromosome 22, trisomy: A very rare disorder where there is an extra copy of chromosome 22 in all the body cells. The condition is usually fatal soon after birth or during the fetal stage. More detailed information about the symptoms, causes, and treatments of Chromosome 22, trisomy is available below.

Symptoms of Chromosome 22, trisomy

Home Diagnostic Testing

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Chromosome 22, trisomy: Complications

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Causes of Chromosome 22, trisomy

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Disease Topics Related To Chromosome 22, trisomy

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Chromosome 22, trisomy: Research Doctors & Specialists

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Hospitals & Clinics: Chromosome 22, trisomy

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Choosing the Best Hospital: More general information, not necessarily in relation to Chromosome 22, trisomy, on hospital performance and surgical care quality:

Statistics for Chromosome 22, trisomy

Chromosome 22, trisomy: Broader Related Topics

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Definitions of Chromosome 22, trisomy:

Chromosome 22, trisomy is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Chromosome 22, trisomy, or a subtype of Chromosome 22, trisomy, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

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More information about Chromosome 22, trisomy

  1. Chromosome 22, trisomy: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Home Testing
  6. Complications
 

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