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Stickler Syndrome, type I

Stickler Syndrome, type I: Introduction

Stickler Syndrome, type I: A rare genetic disorder characterized by joint problems, distinctive facial characteristics and eye and ear abnormalities. Type 1 is caused by a genetic defect on chromosome 12q13.11-q13.2. More detailed information about the symptoms, causes, and treatments of Stickler Syndrome, type I is available below.

Symptoms of Stickler Syndrome, type I

Home Diagnostic Testing

Home medical testing related to Stickler Syndrome, type I:

Wrongly Diagnosed with Stickler Syndrome, type I?

Stickler Syndrome, type I: Complications

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

Causes of Stickler Syndrome, type I

Read more about causes of Stickler Syndrome, type I.

Less Common Symptoms of Stickler Syndrome, type I

Stickler Syndrome, type I: Undiagnosed Conditions

Commonly undiagnosed diseases in related medical categories:

Misdiagnosis and Stickler Syndrome, type I

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

Stickler Syndrome, type I: Research Doctors & Specialists

Research related physicians and medical specialists:

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Evidence Based Medicine Research for Stickler Syndrome, type I

Medical research articles related to Stickler Syndrome, type I include:

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Stickler Syndrome, type I: Animations

Research about Stickler Syndrome, type I

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Stickler Syndrome, type I: Broader Related Topics

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Related Stickler Syndrome, type I Info

More information about Stickler Syndrome, type I

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

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