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Multiple synostoses syndrome 1

Multiple synostoses syndrome 1: Introduction

Multiple synostoses syndrome 1: A rare genetic disorder characterized by deafness, distinctive facial features and fusion of various bones in the fingers, toes and upper arms. More detailed information about the symptoms, causes, and treatments of Multiple synostoses syndrome 1 is available below.

Symptoms of Multiple synostoses syndrome 1

Wrongly Diagnosed with Multiple synostoses syndrome 1?

Multiple synostoses syndrome 1: Complications

Read more about complications of Multiple synostoses syndrome 1.

Causes of Multiple synostoses syndrome 1

Read more about causes of Multiple synostoses syndrome 1.

Misdiagnosis and Multiple synostoses syndrome 1

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Multiple synostoses syndrome 1: Research Doctors & Specialists

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Multiple synostoses syndrome 1: Animations

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Definitions of Multiple synostoses syndrome 1:

Multiple synostoses syndrome 1 is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Multiple synostoses syndrome 1, or a subtype of Multiple synostoses syndrome 1, 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 Multiple synostoses syndrome 1 as a "rare disease".
Source - Orphanet

Related Multiple synostoses syndrome 1 Info

More information about Multiple synostoses syndrome 1

  1. Multiple synostoses syndrome 1: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Misdiagnosis
  6. Complications
 

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