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Goldenhar Syndrome

Goldenhar Syndrome: Introduction

Goldenhar Syndrome: A congenital condition which affects the eyes, ears and vertebrae. More detailed information about the symptoms, causes, and treatments of Goldenhar Syndrome is available below.

Symptoms of Goldenhar Syndrome

  • Underdeveloped cheeks - often only one side affected
  • Underdeveloped upper jaw - often only one side affected
  • Underdeveloped lower jaw - often only one side affected
  • Lateral cleft-like extension of corner of mouth - often only one side affected
  • Underdeveloped face muscles - often only one side affected
  • more symptoms...»

Home Diagnostic Testing

Home medical testing related to Goldenhar Syndrome:

Wrongly Diagnosed with Goldenhar Syndrome?

Goldenhar Syndrome: Related Patient Stories

Goldenhar Syndrome: Complications

Read more about complications of Goldenhar Syndrome.

Causes of Goldenhar Syndrome

Read more about causes of Goldenhar Syndrome.

Disease Topics Related To Goldenhar Syndrome

Research the causes of these diseases that are similar to, or related to, Goldenhar Syndrome:

Goldenhar Syndrome: Undiagnosed Conditions

Commonly undiagnosed diseases in related medical categories:

Goldenhar Syndrome: Research Doctors & Specialists

Research related physicians and medical specialists:

Other doctor, physician and specialist research services:

Evidence Based Medicine Research for Goldenhar Syndrome

Medical research articles related to Goldenhar Syndrome include:

Click here to find more evidence-based articles on the TRIP Database

Goldenhar Syndrome: Animations

Research about Goldenhar Syndrome

Visit our research pages for current research about Goldenhar Syndrome treatments.

Statistics for Goldenhar Syndrome

Goldenhar Syndrome: Broader Related Topics

User Interactive Forums

Read about other experiences, ask a question about Goldenhar Syndrome, or answer someone else's question, on our message boards:

Definitions of Goldenhar Syndrome:

A complex syndrome characterized mainly by aural, oral, and mandibular developmental anomalies which may vary from mild to severe and frequently involve one side of the body. Vertebral anomalies, epibulbar epidermoids, mental retardation, and numerous other anomalies are frequently associated. Orofacial anomalies differ from those in mandibulofacial dysostosis which are usually symmetrical. The presence of hypertelorism may indicate aneuploidy. - (Source - Diseases Database)

Goldenhar Syndrome is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Goldenhar Syndrome, or a subtype of Goldenhar Syndrome, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

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

 

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