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Pseudotrisomy 13 syndrome

Pseudotrisomy 13 syndrome: Introduction

Pseudotrisomy 13 syndrome: A very rare chromosomal disorder characterized mainly by abnormal forebrain development (holoprosencephaly), underdeveloped midface and extra fingers. More detailed information about the symptoms, causes, and treatments of Pseudotrisomy 13 syndrome is available below.

Symptoms of Pseudotrisomy 13 syndrome

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Causes of Pseudotrisomy 13 syndrome

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Less Common Symptoms of Pseudotrisomy 13 syndrome

Pseudotrisomy 13 syndrome: Research Doctors & Specialists

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Hospitals & Clinics: Pseudotrisomy 13 syndrome

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Statistics for Pseudotrisomy 13 syndrome

Pseudotrisomy 13 syndrome: Broader Related Topics

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Definitions of Pseudotrisomy 13 syndrome:

Pseudotrisomy 13 syndrome is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Pseudotrisomy 13 syndrome, or a subtype of Pseudotrisomy 13 syndrome, 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 Pseudotrisomy 13 syndrome as a "rare disease".
Source - Orphanet

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More information about Pseudotrisomy 13 syndrome

  1. Pseudotrisomy 13 syndrome: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Home Testing
 

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