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Diseases » Frias syndrome » Summary
 

What is Frias syndrome?

What is Frias syndrome?

  • Frias syndrome: A rare syndrome characterized mainly by short stature, short fingers and toes and facial anomalies.

Ophanet, a consortium of European partners, currently defines a condition rare when it affects 1 person per 2,000. They list Frias syndrome as a "rare disease".
Source - Orphanet

Frias syndrome: Introduction

Types of Frias syndrome:

Broader types of Frias syndrome:

What causes Frias syndrome?

Causes of Frias syndrome: see causes of Frias syndrome

What are the symptoms of Frias syndrome?

Symptoms of Frias syndrome: see symptoms of Frias syndrome

Frias syndrome: Testing

Diagnostic testing: see tests for Frias syndrome.

Misdiagnosis: see misdiagnosis and Frias syndrome.

How is it treated?

Doctors and Medical Specialists for Frias syndrome: Medical Geneticist ; see also doctors and medical specialists for Frias syndrome.
Treatments for Frias syndrome: see treatments for Frias syndrome

Name and Aliases of Frias syndrome

Main name of condition: Frias syndrome

Other names or spellings for Frias syndrome:

Growth deficiency [brachydactyly - dysmorphism]

 

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