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Craniofrontonasal dysplasia

Craniofrontonasal dysplasia: Introduction

Craniofrontonasal dysplasia: A rare genetic disorder mainly found in females and characterized by premature closing of skull bones and craniofacial and limb abnormalities. More detailed information about the symptoms, causes, and treatments of Craniofrontonasal dysplasia is available below.

Symptoms of Craniofrontonasal dysplasia

  • Premature closing of skull bones #in females
  • Brachycephaly #in females
  • Frontal bossing #in males
  • Increased bony interorbital distance #in males
  • Widely spaced eyes
  • more symptoms...»

Causes of Craniofrontonasal dysplasia

Read more about causes of Craniofrontonasal dysplasia.

Disease Topics Related To Craniofrontonasal dysplasia

Research the causes of these diseases that are similar to, or related to, Craniofrontonasal dysplasia:

Less Common Symptoms of Craniofrontonasal dysplasia

  • Telecanthus #females
  • Exotropia #females
  • Nystagmus #females
  • Strabismus #females
  • Sprengel deformity #females
  • more symptoms...»

Evidence Based Medicine Research for Craniofrontonasal dysplasia

Medical research articles related to Craniofrontonasal dysplasia include:

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

Craniofrontonasal dysplasia: Animations

Research about Craniofrontonasal dysplasia

Visit our research pages for current research about Craniofrontonasal dysplasia treatments.

Statistics for Craniofrontonasal dysplasia

Craniofrontonasal dysplasia: Broader Related Topics

User Interactive Forums

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Definitions of Craniofrontonasal dysplasia:

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

Related Craniofrontonasal dysplasia Info

More information about Craniofrontonasal dysplasia

  1. Craniofrontonasal dysplasia: Introduction
  2. Symptoms
  3. Causes
  4. Treatments

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