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Stickler Syndrome, type II

Stickler Syndrome, type II: Introduction

Stickler Syndrome, type II: A rare genetic disorder characterized by joint problems, distinctive facial characteristics and eye and ear abnormalities. Type 2 is caused by a genetic defect on chromosome 1p21. More detailed information about the symptoms, causes, and treatments of Stickler Syndrome, type II is available below.

Symptoms of Stickler Syndrome, type II

Home Diagnostic Testing

Home medical testing related to Stickler Syndrome, type II:

Wrongly Diagnosed with Stickler Syndrome, type II?

Stickler Syndrome, type II: Complications

Review possible medical complications related to Stickler Syndrome, type II:

Causes of Stickler Syndrome, type II

Read more about causes of Stickler Syndrome, type II.

Less Common Symptoms of Stickler Syndrome, type II

Stickler Syndrome, type II: Undiagnosed Conditions

Commonly undiagnosed diseases in related medical categories:

Misdiagnosis and Stickler Syndrome, type II

Psoriatic arthritis often undiagnosed cause of joint conditions: Patients with the skin condition psoriasis can also have the related...read more »

Stickler Syndrome, type II: Research Doctors & Specialists

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Stickler Syndrome, type II: Animations

Stickler Syndrome, type II: Broader Related Topics

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Related Stickler Syndrome, type II Info

More information about Stickler Syndrome, type II

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

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