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Apert syndrome

Apert syndrome: Introduction

Apert syndrome: A rare condition characterized by abnormalities in the appearance of the face and head as well as finger and toe abnormalities. The bones of the skull fuse together too early which prevents it from growing normally. Various toes and fingers may be fused together. More detailed information about the symptoms, causes, and treatments of Apert syndrome is available below.

Symptoms of Apert syndrome

  • Partially or totally joined fingers
  • Partially or totally joined toes
  • Premature joining of bones in the head
  • Growth disturbance in the skull
  • Long-shaped head
  • more symptoms...»

Treatments for Apert syndrome

  • Surgery may be needed to prevent premature skull bone fusion from causing damage to the brain. Surgery is also needed to separate the fused fingers and toes and to correct any other defects if they become a problem. Orthodontic work is also often required. Other treatments are advised as symptoms develop
  • more treatments...»

Wrongly Diagnosed with Apert syndrome?

Apert syndrome: Related Patient Stories

Apert syndrome: Complications

Review possible medical complications related to Apert syndrome:

  • Premature closure of skull bones can result in increased pressure inside the skull which in turn can result in mental retardation
  • more complications...»

Causes of Apert syndrome

Read more about causes of Apert syndrome.

Disease Topics Related To Apert syndrome

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

Less Common Symptoms of Apert syndrome

Misdiagnosis and Apert syndrome

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Apert syndrome: Research Doctors & Specialists

Research related physicians and medical specialists:

Other doctor, physician and specialist research services:

Evidence Based Medicine Research for Apert syndrome

Medical research articles related to Apert syndrome include:

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

Apert syndrome: Animations

Prognosis for Apert syndrome

Prognosis for Apert syndrome: The prognosis varies amongst patients depending on the severity and range of symptoms. Early diagnosis and management of the condition with surgical intervention as required allows for a better prognosis.

Research about Apert syndrome

Visit our research pages for current research about Apert syndrome treatments.

Statistics for Apert syndrome

Apert syndrome: Broader Related Topics

User Interactive Forums

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

Definitions of Apert syndrome:

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

 

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