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ACPS III: Introduction

ACPS 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 ACPS III is available below.

Symptoms of ACPS III

Wrongly Diagnosed with ACPS III?

Causes of ACPS III

Read more about causes of ACPS III.

Misdiagnosis and ACPS III

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ACPS III: Research Doctors & Specialists

Research related physicians and medical specialists:

Other doctor, physician and specialist research services:

ACPS III: Animations

Statistics for ACPS III

ACPS III: Broader Related Topics

User Interactive Forums

Read about other experiences, ask a question about ACPS III, or answer someone else's question, on our message boards:

Definitions of ACPS III:

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

Related ACPS III Info

More information about ACPS III

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

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