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Acrocephalopolysyndactyly type III

Acrocephalopolysyndactyly type III: Introduction

Acrocephalopolysyndactyly type III: A rare genetic condition characterized by head and digital anomalies as well as other abnormalities. More detailed information about the symptoms, causes, and treatments of Acrocephalopolysyndactyly type III is available below.

Symptoms of Acrocephalopolysyndactyly type III

Wrongly Diagnosed with Acrocephalopolysyndactyly type III?

Causes of Acrocephalopolysyndactyly type III

Read more about causes of Acrocephalopolysyndactyly type III.

Misdiagnosis and Acrocephalopolysyndactyly type III

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Acrocephalopolysyndactyly type III: Research Doctors & Specialists

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Acrocephalopolysyndactyly type III: Animations

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Acrocephalopolysyndactyly type III: Broader Related Topics

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Definitions of Acrocephalopolysyndactyly type III:

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

Related Acrocephalopolysyndactyly type III Info

More information about Acrocephalopolysyndactyly type III

  1. Acrocephalopolysyndactyly type III: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Misdiagnosis
 

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