Craniofrontonasal dysplasia is caused by a gene on the X-chromosome. It can occur spontaneously or can be inherited in an X-linked pattern. Interestingly, unlike most X-linked conditions, it affects females more significantly than males. The cause of Tessier clefts is not yet known.
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Craniofrontonasal dysplasia (CFND) is a very rare inherited disorder characterized by body – especially facial – asymmetry, midline defects, skeletal ...
Jan 1, 2020 · Craniofrontonasal syndrome is a rare condition characterized by the premature closure of certain bones of the skull (craniosynostosis) ...
Craniofrontonasal dysplasia is a rare genetic condition with several skeletal defects. Main features of this condition include widely spaced eyes ...
![PDF] Surgical approach of hypertelorbitism in craniofrontonasal ...](https://www.google.com/imgres?imgurl=https://d3i71xaburhd42.cloudfront.net/7e8cad3d222dbf15813f0d8f11550687ae3ee3ce/4-Figure2-1.png&imgrefurl=https://www.semanticscholar.org/paper/Surgical-approach-of-hypertelorbitism-in-dysplasia.-Denadai-Roberto/7e8cad3d222dbf15813f0d8f11550687ae3ee3ce&h=984&w=674&tbnid=k4gWFBTTJMy0gM&q=Craniofrontonasal+Dysplasia&tbnh=149&tbnw=102&usg=AI4_-kQREjLTNrlqA3iKxOGsKy1s5P817w&vet=1&docid=6a8vwoQUhJbH7M&hl=en&client=pub-1787672658759074&sa=X&ved=2ahUKEwiYrtv69-2FAxXJv4kEHRPJC8IQ9QF6BAgMEA4)
A rare X-linked malformation syndrome characterized by craniofacial abnormalities such as uni- or bicoronal synostosis, hypertelorism and a bifid nose, grooved ...
Craniofrontonasal syndrome is an X-linked developmental disorder that shows paradoxically greater severity in heterozygous females than in hemizygous males.
Craniofrontonasal dysplasia is a very rare X-linked malformation syndrome caused by mutations in the ephrin-B1 gene (EFNB1). Phenotypic expression varies ...
Craniofrontonasal syndrome is an X-linked developmental disorder that shows paradoxically greater severity in heterozygous females than in hemizygous males.
Cranio-fronto-nasal dysplasia is a genetic condition, caused by a mutation (change) on a specific gene. Research has identified the affected gene as the EFNB1 ...
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