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Chromosome 17, trisomy 17p11.2

Chromosome 17, trisomy 17p11.2: Introduction

Chromosome 17, trisomy 17p11.2: A rare chromosomal disorder where a portion of the short arm of chromosome 17 is duplicated. More detailed information about the symptoms, causes, and treatments of Chromosome 17, trisomy 17p11.2 is available below.

Symptoms of Chromosome 17, trisomy 17p11.2

Home Diagnostic Testing

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Causes of Chromosome 17, trisomy 17p11.2

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Chromosome 17, trisomy 17p11.2: Research Doctors & Specialists

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Hospitals & Clinics: Chromosome 17, trisomy 17p11.2

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Statistics for Chromosome 17, trisomy 17p11.2

Chromosome 17, trisomy 17p11.2: Broader Related Topics

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Definitions of Chromosome 17, trisomy 17p11.2:

Chromosome 17, trisomy 17p11.2 is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Chromosome 17, trisomy 17p11.2, or a subtype of Chromosome 17, trisomy 17p11.2, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

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More information about Chromosome 17, trisomy 17p11.2

  1. Chromosome 17, trisomy 17p11.2: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Home Testing
 

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