Skip to main content

Link path

MeSH Tree Location(s) for Craniofacial Dysostosis

Scope Note:
Autosomal dominant CRANIOSYNOSTOSIS with shallow ORBITS; EXOPHTHALMOS; and maxillary hypoplasia.

Förklaring:
En autosomalt dominant missbildning, kännetecknad av akrocefali (spetsig skalle), exoftalmus (utstående ögon), hypertelorism (stort avstånd mellan ögonen), strabismus (skelögdhet), papegojnäsa, liten underkäke och utskjutande överkäke.

See also: Receptor, Fibroblast Growth Factor, Type 2


Location corresponding to Mesh Number C05.116.099.370.231

Dysostoses  Benbildningsdefekter
Dysostoser
Craniofacial Dysostosis   Kraniofacial dysostos
Crouzons sjukdom
Hallermann's Syndrome   Hallermanns syndrom
Hypertelorism   Hypertelorism
Mandibulofacial Dysostosis+   Mandibulofacial dysostos
Treacher Collins syndrom
Location corresponding to Mesh Number C05.660.207.231

Craniofacial Abnormalities  Kraniofaciala missbildningar
Craniofacial Dysostosis   Kraniofacial dysostos
Crouzons sjukdom
Hallermann's Syndrome   Hallermanns syndrom
Hypertelorism   Hypertelorism
Mandibulofacial Dysostosis+   Mandibulofacial dysostos
Treacher Collins syndrom
Location corresponding to Mesh Number C16.131.621.207.231

Craniofacial Abnormalities  Kraniofaciala missbildningar
Craniofacial Dysostosis   Kraniofacial dysostos
Crouzons sjukdom
Hallermann's Syndrome   Hallermanns syndrom
Hypertelorism   Hypertelorism
Mandibulofacial Dysostosis+   Mandibulofacial dysostos
Treacher Collins syndrom
MeSH Start Page
© Karolinska Institutet University Library 1998. Last modified 2013-01-31.