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Pashayan syndrome

Pashayan syndrome: Introduction

Pashayan syndrome: A rare inherited condition characterized mainly by eye, nose and facial malformations. More detailed information about the symptoms, causes, and treatments of Pashayan syndrome is available below.

Symptoms of Pashayan syndrome

Home Diagnostic Testing

Home medical testing related to Pashayan syndrome:

Wrongly Diagnosed with Pashayan syndrome?

Causes of Pashayan syndrome

Read more about causes of Pashayan syndrome.

Disease Topics Related To Pashayan syndrome

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Pashayan syndrome: Undiagnosed Conditions

Commonly undiagnosed diseases in related medical categories:

Pashayan syndrome: Research Doctors & Specialists

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Pashayan syndrome: Animations

Statistics for Pashayan syndrome

Pashayan syndrome: Broader Related Topics

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Definitions of Pashayan syndrome:

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

Related Pashayan syndrome Info

More information about Pashayan syndrome

  1. Pashayan syndrome: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Misdiagnosis
  6. Home Testing
 

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