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What is Chromosome 14 trisomy?

What is Chromosome 14 trisomy?

  • Chromosome 14 trisomy: A rare chromosomal disorder involving duplication of genetic material from chromosome 14 resulting in various abnormalities. The type and severity of symptoms varies depending on the amount and exact location of the genetic material that is duplicated.

Chromosome 14 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 14 trisomy, or a subtype of Chromosome 14 trisomy, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

Chromosome 14 trisomy: Introduction

Types of Chromosome 14 trisomy:

Broader types of Chromosome 14 trisomy:

How serious is Chromosome 14 trisomy?

Prognosis of Chromosome 14 trisomy: The prognosis varies depending on the type and severity of symptoms that develop. Prompt diagnosis and appropriate treatment can improve prognosis and quality of life.
Complications of Chromosome 14 trisomy: see complications of Chromosome 14 trisomy

What causes Chromosome 14 trisomy?

Causes of Chromosome 14 trisomy: see causes of Chromosome 14 trisomy

What are the symptoms of Chromosome 14 trisomy?

Symptoms of Chromosome 14 trisomy: see symptoms of Chromosome 14 trisomy

Complications of Chromosome 14 trisomy: see complications of Chromosome 14 trisomy

Chromosome 14 trisomy: Testing

Diagnostic testing: see tests for Chromosome 14 trisomy.

How is it treated?

Doctors and Medical Specialists for Chromosome 14 trisomy: Medical Geneticist ; see also doctors and medical specialists for Chromosome 14 trisomy.
Treatments for Chromosome 14 trisomy: see treatments for Chromosome 14 trisomy

Name and Aliases of Chromosome 14 trisomy

Main name of condition: Chromosome 14 trisomy

Other names or spellings for Chromosome 14 trisomy:

Trisomy 14

Trisomy 14
Source - Office of Rare Diseases (ORD) of the National Institutes of Health (NIH)

 

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