Craniofrontonasal Dysplasia

Below you will find more information about Craniofrontonasal Dysplasia from Medigest. If you believe that you are suffering from any of the symptoms of Craniofrontonasal Dysplasia it is important that you obtain an accurate diagnosis from a medical professional to ensure that you obtain the correct medication or treatment for your condition. There are medical conditions that carry similar symptoms associated with Craniofrontonasal Dysplasia and therefore the information provided by Medigest is offered as a guideline only and should never be used in preference to seeking professional medical advice. The information relating to Craniofrontonasal Dysplasia comes from a third party source and Medigest will not be held liable for any inaccuracies relating to the information shown.


Craniofrontonasal dysplasia is a rare genetic disorder characterized by an abnormal structure of the head and face, as well as the hands, feet and some skeletal bones. Among the symptoms of the disorder are widely spaced eyes, a cleft structure on the nose, an abnormally wide mouth, deformities in the fingers and toes, and sometimes underdeveloped parts of the face. The skull may as well suffer from certain malformations due to the premature joining of the sutures. It is currently described as an autosomal dominant disorder.

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