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Diseases » Duplication 10p » Summary

What is Duplication 10p?

What is Duplication 10p?

  • Duplication 10p: A rare chromosomal disorder where there are three copies of the short arm (p) of chromosome 10 rather than the normal two resulting in various abnormalities. The type and severity of symptoms depend on the amount and location of genetic material duplicated.

Duplication 10p is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Duplication 10p, or a subtype of Duplication 10p, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

Ophanet, a consortium of European partners, currently defines a condition rare when it affects 1 person per 2,000. They list Duplication 10p as a "rare disease".
Source - Orphanet

Duplication 10p: Introduction

Types of Duplication 10p:

Broader types of Duplication 10p:

How serious is Duplication 10p?

Prognosis of Duplication 10p: 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.

What causes Duplication 10p?

Causes of Duplication 10p: see causes of Duplication 10p

What are the symptoms of Duplication 10p?

Symptoms of Duplication 10p: see symptoms of Duplication 10p

How is it treated?

Doctors and Medical Specialists for Duplication 10p: Medical Geneticist ; see also doctors and medical specialists for Duplication 10p.
Treatments for Duplication 10p: see treatments for Duplication 10p

Name and Aliases of Duplication 10p

Main name of condition: Duplication 10p

Other names or spellings for Duplication 10p:

Trisomy 10p, Chromosome 10, trisomy 10p
Source - Office of Rare Diseases (ORD) of the National Institutes of Health (NIH)


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