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Arthrogryposis multiplex congenita, distal, X-linked

Arthrogryposis multiplex congenita, distal, X-linked: Introduction

Arthrogryposis multiplex congenita, distal, X-linked: A rare condition characterized by the presence of contractures at birth as well as various other anomalies. The condition is X-linked. More detailed information about the symptoms, causes, and treatments of Arthrogryposis multiplex congenita, distal, X-linked is available below.

Symptoms of Arthrogryposis multiplex congenita, distal, X-linked

Wrongly Diagnosed with Arthrogryposis multiplex congenita, distal, X-linked?

Causes of Arthrogryposis multiplex congenita, distal, X-linked

Read more about causes of Arthrogryposis multiplex congenita, distal, X-linked.

Less Common Symptoms of Arthrogryposis multiplex congenita, distal, X-linked

Misdiagnosis and Arthrogryposis multiplex congenita, distal, X-linked

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Arthrogryposis multiplex congenita, distal, X-linked: Research Doctors & Specialists

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Arthrogryposis multiplex congenita, distal, X-linked: Broader Related Topics

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Definitions of Arthrogryposis multiplex congenita, distal, X-linked:

Arthrogryposis multiplex congenita, distal, X-linked is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Arthrogryposis multiplex congenita, distal, X-linked, or a subtype of Arthrogryposis multiplex congenita, distal, X-linked, 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 Arthrogryposis multiplex congenita, distal, X-linked as a "rare disease".
Source - Orphanet

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More information about Arthrogryposis multiplex congenita, distal, X-linked

  1. Arthrogryposis multiplex congenita, distal, X-linked: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Misdiagnosis
 

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