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Craniosynostosis Maroteaux Fonfria type

Craniosynostosis Maroteaux Fonfria type: Introduction

Craniosynostosis Maroteaux Fonfria type: A rare disorder which is similar to a condition called Apert syndrome but also involves extra fingers and toes. Apert syndrome is 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. More detailed information about the symptoms, causes, and treatments of Craniosynostosis Maroteaux Fonfria type is available below.

Symptoms of Craniosynostosis Maroteaux Fonfria type

  • Extra little finger
  • Extra big toe
  • Partially or totally joined fingers
  • Partially or totally joined toes
  • Premature joining of bones in the head
  • more symptoms...»

Wrongly Diagnosed with Craniosynostosis Maroteaux Fonfria type?

Causes of Craniosynostosis Maroteaux Fonfria type

Read more about causes of Craniosynostosis Maroteaux Fonfria type.

Less Common Symptoms of Craniosynostosis Maroteaux Fonfria type

Misdiagnosis and Craniosynostosis Maroteaux Fonfria type

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Craniosynostosis Maroteaux Fonfria type: Research Doctors & Specialists

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More information about Craniosynostosis Maroteaux Fonfria type

  1. Craniosynostosis Maroteaux Fonfria type: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Misdiagnosis
 

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