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Duplication 10p

Duplication 10p: Introduction

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. More detailed information about the symptoms, causes, and treatments of Duplication 10p is available below.

Symptoms of Duplication 10p

Treatments for Duplication 10p

  • Treatment varies depending on the type and severity of symptom that develop
  • Surgery may be needed to correct defects or abnormalities e.g. cleft palate, undescended testes
  • Access to programs and services as required e.g. physical therapy, speech therapy, educational support, social, vocational and medical services
  • Various symptomatic and supportive measures as required
  • Genetic counseling and joining a support group is recommended
  • more treatments...»

Causes of Duplication 10p

Read more about causes of Duplication 10p.

Prognosis for Duplication 10p

Prognosis for 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.

Statistics for Duplication 10p

Duplication 10p: Broader Related Topics

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Definitions of Duplication 10p:

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

Related Duplication 10p Info

Videos about Duplication 10p

 

More information about Duplication 10p

  1. Duplication 10p: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Prognosis
 

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