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What is Chromosome 20, trisomy?

What is Chromosome 20, trisomy?

  • Chromosome 20, trisomy: A rare chromosomal disorder where there are three copies of chromosome 20 rather than the normal two which results in severe abnormalities and death.

Chromosome 20, 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 20, trisomy, or a subtype of Chromosome 20, trisomy, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

Chromosome 20, trisomy: Introduction

Types of Chromosome 20, trisomy:

Broader types of Chromosome 20, trisomy:

What causes Chromosome 20, trisomy?

Causes of Chromosome 20, trisomy: see causes of Chromosome 20, trisomy

What are the symptoms of Chromosome 20, trisomy?

Symptoms of Chromosome 20, trisomy: see symptoms of Chromosome 20, trisomy

Chromosome 20, trisomy: Testing

Diagnostic testing: see tests for Chromosome 20, trisomy.

How is it treated?

Doctors and Medical Specialists for Chromosome 20, trisomy: Medical Geneticist ; see also doctors and medical specialists for Chromosome 20, trisomy.
Treatments for Chromosome 20, trisomy: see treatments for Chromosome 20, trisomy

Name and Aliases of Chromosome 20, trisomy

Main name of condition: Chromosome 20, trisomy

Other names or spellings for Chromosome 20, trisomy:

Trisomy 20 mosaicism, Trisomy 20, Chromosome 20 duplication

Chromosome 20 duplication, Trisomy 20, Trisomy 20 mosaicism
Source - Office of Rare Diseases (ORD) of the National Institutes of Health (NIH)

Chromosome 20, trisomy: Related Conditions

Research the causes of these diseases that are similar to, or related to, Chromosome 20, trisomy:

  • Rrae chromosomal disorder
  • Facial deformity
  • Spinal dysplasia
  • Gastrointestinal anomalies
  • Multiple congenital malformations
 

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