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Ablepharon macrostomia syndrome

Ablepharon macrostomia syndrome: Introduction

Ablepharon macrostomia syndrome: A rare disorder involving a number of mainly physical abnormalities. More detailed information about the symptoms, causes, and treatments of Ablepharon macrostomia syndrome is available below.

Symptoms of Ablepharon macrostomia syndrome

See full list of 22 symptoms of Ablepharon macrostomia syndrome

Ablepharon macrostomia syndrome: Complications

Read more about complications of Ablepharon macrostomia syndrome.

Disease Topics Related To Ablepharon macrostomia syndrome

Research the causes of these diseases that are similar to, or related to, Ablepharon macrostomia syndrome:

Less Common Symptoms of Ablepharon macrostomia syndrome

Read more about symptoms of Ablepharon macrostomia syndrome

Treatments for Ablepharon macrostomia syndrome

  • Treatment usually involves plastic and reconstructive surgery. Surgery may be needed to correct undescended testes or hernias
  • more treatments...»

Read more about treatments for Ablepharon macrostomia syndrome

Evidence Based Medicine Research for Ablepharon macrostomia syndrome

Medical research articles related to Ablepharon macrostomia syndrome include:

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

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Prognosis for Ablepharon macrostomia syndrome

Prognosis for Ablepharon macrostomia syndrome: The prognosis is usually poor.

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Reseach about Ablepharon macrostomia syndrome

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User Interactive Forums

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Definitions of Ablepharon macrostomia syndrome:

Ablepharon macrostomia syndrome is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Ablepharon macrostomia syndrome, or a subtype of Ablepharon macrostomia 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 Ablepharon macrostomia syndrome as a "rare disease".
Source - Orphanet


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