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Axenfeld-Rieger syndrome

Axenfeld-Rieger syndrome: Introduction

Axenfeld-Rieger syndrome: A rare genetic disorder characterized by underdeveloped or absent teeth and craniofacial and eye abnormalities. The range of symptoms that can occur is somewhat variable. More detailed information about the symptoms, causes, and treatments of Axenfeld-Rieger syndrome is available below.

Symptoms of Axenfeld-Rieger syndrome

Home Diagnostic Testing

Home medical testing related to Axenfeld-Rieger syndrome:

Wrongly Diagnosed with Axenfeld-Rieger syndrome?

Causes of Axenfeld-Rieger syndrome

More information about causes of Axenfeld-Rieger syndrome:

Less Common Symptoms of Axenfeld-Rieger syndrome

Axenfeld-Rieger syndrome: Undiagnosed Conditions

Commonly undiagnosed diseases in related medical categories:

Axenfeld-Rieger syndrome: Research Doctors & Specialists

Research related physicians and medical specialists:

Other doctor, physician and specialist research services:

Hospitals & Clinics: Axenfeld-Rieger syndrome

Research quality ratings and patient safety measures for medical facilities in specialties related to Axenfeld-Rieger syndrome:

Choosing the Best Hospital: More general information, not necessarily in relation to Axenfeld-Rieger syndrome, on hospital performance and surgical care quality:

Axenfeld-Rieger syndrome: Animations

Statistics for Axenfeld-Rieger syndrome

Axenfeld-Rieger syndrome: Broader Related Topics

User Interactive Forums

Read about other experiences, ask a question about Axenfeld-Rieger syndrome, or answer someone else's question, on our message boards:

Definitions of Axenfeld-Rieger syndrome:

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

Related Axenfeld-Rieger syndrome Info

More information about Axenfeld-Rieger syndrome

  1. Axenfeld-Rieger syndrome: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Misdiagnosis
  6. Home Testing

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