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Monosomy 20p

Monosomy 20p: Introduction

Monosomy 20p: A rare chromosomal disorder where the short arm (p) of chromosome 20 is deleted resulting in various abnormalities. The type and severity of symptoms varies depending on the amount and exact location of the genetic material that is deleted. More detailed information about the symptoms, causes, and treatments of Monosomy 20p is available below.

Symptoms of Monosomy 20p

Treatments for Monosomy 20p

  • Treatment varies depending on the type and severity of symptom that develop
  • Surgery may be needed to correct defects or abnormalities e.g. heart defects
  • 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 Monosomy 20p

Read more about causes of Monosomy 20p.

Prognosis for Monosomy 20p

Prognosis for Monosomy 20p: 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 Monosomy 20p

Monosomy 20p: Broader Related Topics

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Definitions of Monosomy 20p:

Monosomy 20p is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Monosomy 20p, or a subtype of Monosomy 20p, 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 Monosomy 20p as a "rare disease".
Source - Orphanet

Related Monosomy 20p Info

Videos about Monosomy 20p

 

More information about Monosomy 20p

  1. Monosomy 20p: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Prognosis
 

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