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Stickler Syndrome, type III

Stickler Syndrome, type III: Introduction

Stickler Syndrome, type III: A rare genetic disorder characterized by joint problems, distinctive facial characteristics and ear abnormalities. Type 3 is caused by a genetic defect on chromosome 6q21.3. Type 3 doesn't involve any of the eye problems that occur in type 1 and 2. More detailed information about the symptoms, causes, and treatments of Stickler Syndrome, type III is available below.

Symptoms of Stickler Syndrome, type III

Home Diagnostic Testing

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Wrongly Diagnosed with Stickler Syndrome, type III?

Stickler Syndrome, type III: Complications

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Causes of Stickler Syndrome, type III

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Less Common Symptoms of Stickler Syndrome, type III

Misdiagnosis and Stickler Syndrome, type III

Psoriatic arthritis often undiagnosed cause of joint conditions: Patients with the skin condition psoriasis can also have the related arthritis subtype called "psoriatic arthritis". This arthritic condition tends to be...read more »

Stickler Syndrome, type III: Research Doctors & Specialists

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Stickler Syndrome, type III: Animations

Stickler Syndrome, type III: Broader Related Topics

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Related Stickler Syndrome, type III Info

More information about Stickler Syndrome, type III

  1. Stickler Syndrome, type III: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Misdiagnosis
  6. Home Testing
  7. Complications
 

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