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Craniosynostosis Philadelphia type

Craniosynostosis Philadelphia type: Introduction

Craniosynostosis Philadelphia type: A rare disorder characterized primarily by the premature fusion of several skull bones as well as the incomplete separation of fingers and toes (syndactyly). The condition has been reported in five generations of one family. More detailed information about the symptoms, causes, and treatments of Craniosynostosis Philadelphia type is available below.

Symptoms of Craniosynostosis Philadelphia type

Causes of Craniosynostosis Philadelphia type

Read more about causes of Craniosynostosis Philadelphia type.

Disease Topics Related To Craniosynostosis Philadelphia type

Research the causes of these diseases that are similar to, or related to, Craniosynostosis Philadelphia type:

Statistics for Craniosynostosis Philadelphia type

Craniosynostosis Philadelphia type: Broader Related Topics

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Definitions of Craniosynostosis Philadelphia type:

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

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More information about Craniosynostosis Philadelphia type

  1. Craniosynostosis Philadelphia type: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
 

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