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What is Chromosome 22, trisomy?

What is Chromosome 22, trisomy?

  • 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.

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)

Chromosome 22, trisomy: Introduction

Types of Chromosome 22, trisomy:

Broader types of Chromosome 22, trisomy:

How serious is Chromosome 22, trisomy?

Complications of Chromosome 22, trisomy: see complications of Chromosome 22, trisomy

What causes Chromosome 22, trisomy?

Causes of Chromosome 22, trisomy: see causes of Chromosome 22, trisomy

What are the symptoms of Chromosome 22, trisomy?

Symptoms of Chromosome 22, trisomy: see symptoms of Chromosome 22, trisomy

Complications of Chromosome 22, trisomy: see complications of Chromosome 22, trisomy

Chromosome 22, trisomy: Testing

Diagnostic testing: see tests for Chromosome 22, trisomy.

How is it treated?

Doctors and Medical Specialists for Chromosome 22, trisomy: Medical Geneticist ; see also doctors and medical specialists for Chromosome 22, trisomy.
Treatments for Chromosome 22, trisomy: see treatments for Chromosome 22, trisomy

Name and Aliases of Chromosome 22, trisomy

Main name of condition: Chromosome 22, trisomy

Other names or spellings for Chromosome 22, trisomy:

22 trisomy, trisomy 22, Duplication 22

Duplication 22, Trisomy 22
Source - Office of Rare Diseases (ORD) of the National Institutes of Health (NIH)

Chromosome 22, trisomy: Related Conditions

Research the causes of these diseases that are similar to, or related to, Chromosome 22, trisomy:

 

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