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Acrofacial dysostosis, Weyers type

Acrofacial dysostosis, Weyers type: Introduction

Acrofacial dysostosis, Weyers type: A rare disorder characterized by facial abnormalities and extra digits, nail abnormalities and short limbs. More detailed information about the symptoms, causes, and treatments of Acrofacial dysostosis, Weyers type is available below.

Symptoms of Acrofacial dysostosis, Weyers type

  • Extra little finger
  • Extra little toe
  • Fusion of fifth and sixth toes
  • Fusion of fifth and sixth fingers
  • Cleft of mandibular symphysis
  • more symptoms...»

Home Diagnostic Testing

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Wrongly Diagnosed with Acrofacial dysostosis, Weyers type?

Acrofacial dysostosis, Weyers type: Complications

Read more about complications of Acrofacial dysostosis, Weyers type.

Causes of Acrofacial dysostosis, Weyers type

Read more about causes of Acrofacial dysostosis, Weyers type.

Acrofacial dysostosis, Weyers type: Undiagnosed Conditions

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Misdiagnosis and Acrofacial dysostosis, Weyers type

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Acrofacial dysostosis, Weyers type: Research Doctors & Specialists

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Acrofacial dysostosis, Weyers type: Animations

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Definitions of Acrofacial dysostosis, Weyers type:

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

Related Acrofacial dysostosis, Weyers type Info

More information about Acrofacial dysostosis, Weyers type

  1. Acrofacial dysostosis, Weyers type: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Misdiagnosis
  6. Home Testing
  7. Complications
 

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