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- Q779250 subject Q6500135.
- Q779250 subject Q6853484.
- Q779250 subject Q6907472.
- Q779250 subject Q7022834.
- Q779250 subject Q7215483.
- Q779250 subject Q8413581.
- Q779250 abstract "Crouzon syndrome is an autosomal dominant genetic disorder known as a branchial arch syndrome. Specifically, this syndrome affects the first branchial (or pharyngeal) arch, which is the precursor of the maxilla and mandible. Since the branchial arches are important developmental features in a growing embryo, disturbances in their development create lasting and widespread effects.This syndrome is named after Octave Crouzon, a French physician who first described this disorder. He noted the affected patients were a mother and her daughter, implying a genetic basis. First called "craniofacial dysostosis", the disorder was characterized by a number of clinical features. This syndrome is caused by a mutation in the fibroblast growth factor receptor II, located on chromosome 10.Breaking down the name, "craniofacial" refers to the skull and face, and "dysostosis" refers to malformation of bone.Now known as Crouzon syndrome, the disease can be described by the rudimentary meanings of its former name. What occurs in the disease is that an infant's skull and facial bones, while in development, fuse early or are unable to expand. Thus, normal bone growth cannot occur. Fusion of different sutures leads to different patterns of growth of the skull. Examples include: trigonocephaly (fusion of the metopic suture), brachycephaly (fusion of the coronal suture), dolichocephaly (fusion of the sagittal suture), plagiocephaly (unilateral premature closure of lambdoid and coronal sutures), oxycephaly (fusion of coronal and lambdoidal sutures), Kleeblattschaedel (premature closure of all sutures).".
- Q779250 icd10 "Q75.1".
- Q779250 icd9 "756.0".
- Q779250 meshId "D003394".
- Q779250 omim "123500".
- Q779250 thumbnail Patient_with_Crouzon_syndrome_(1912).jpg?width=300.
- Q779250 wikiPageExternalLink crouzon.asp.
- Q779250 wikiPageExternalLink crouzon-syndrome.
- Q779250 wikiPageExternalLink 011804.htm.
- Q779250 wikiPageExternalLink www.cleftadvocate.org.
- Q779250 wikiPageExternalLink www.crouzonsyndrome.org.
- Q779250 wikiPageExternalLink Article.cfm?ArticleID=65&Source=Physician.
- Q779250 wikiPageExternalLink br.fcgi?book=gene&part=craniosynostosis.
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- Q779250 wikiPageWikiLink Q6500135.
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- Q779250 wikiPageWikiLink Q6853484.
- Q779250 wikiPageWikiLink Q6907472.
- Q779250 wikiPageWikiLink Q7022834.
- Q779250 wikiPageWikiLink Q7215483.
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- Q779250 wikiPageWikiLink Q8413581.
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- Q779250 icd "756".
- Q779250 icd "Q75.1".
- Q779250 meshid "D003394".
- Q779250 name "Crouzon syndrome".
- Q779250 omim "123500".
- Q779250 type Disease.
- Q779250 type Thing.
- Q779250 type Q12136.
- Q779250 comment "Crouzon syndrome is an autosomal dominant genetic disorder known as a branchial arch syndrome. Specifically, this syndrome affects the first branchial (or pharyngeal) arch, which is the precursor of the maxilla and mandible. Since the branchial arches are important developmental features in a growing embryo, disturbances in their development create lasting and widespread effects.This syndrome is named after Octave Crouzon, a French physician who first described this disorder.".
- Q779250 label "Crouzon syndrome".
- Q779250 depiction Patient_with_Crouzon_syndrome_(1912).jpg.
- Q779250 name "Crouzon syndrome".