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Johnston Aarons Schelley syndrome

Johnston Aarons Schelley syndrome: Introduction

Johnston Aarons Schelley syndrome: A very rare lethal syndrome characterized mainly by contractures and thickened skin. More detailed information about the symptoms, causes, and treatments of Johnston Aarons Schelley syndrome is available below.

Symptoms of Johnston Aarons Schelley syndrome

Wrongly Diagnosed with Johnston Aarons Schelley syndrome?

Johnston Aarons Schelley syndrome: Complications

Review possible medical complications related to Johnston Aarons Schelley syndrome:

Causes of Johnston Aarons Schelley syndrome

Read more about causes of Johnston Aarons Schelley syndrome.

Misdiagnosis and Johnston Aarons Schelley syndrome

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Johnston Aarons Schelley syndrome: Research Doctors & Specialists

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Johnston Aarons Schelley syndrome: Animations

Statistics for Johnston Aarons Schelley syndrome

Johnston Aarons Schelley syndrome: Broader Related Topics

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Definitions of Johnston Aarons Schelley syndrome:

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

Related Johnston Aarons Schelley syndrome Info

More information about Johnston Aarons Schelley syndrome

  1. Johnston Aarons Schelley syndrome: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Misdiagnosis
  6. Complications
 

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