- Craniofacial abnormality
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"Orafacial abnormality" redirects here. For other orofacial abnormalities, see Mouth disease.
Craniofacial abnormality Classification and external resources 
Human skullICD-10 Q75 ICD-9 756.0 MeSH D019465 Craniofacial abnormalities are congenital musculoskeletal disorders which primarily affect the cranium and facial bones.[1]
They are associated with the development of the pharyngeal arches.[2]
An example is platybasia.
References
External links
- http://embryology.med.unsw.edu.au/Notes/skmus8a.htm
- http://www.hopkinsmedicine.org/craniofacial/LynmProject/BSC/BSC3.HTM
Congenital malformations and deformations of musculoskeletal system / musculoskeletal abnormality (Q65–Q76, 754–756.3) Appendicular
limb / dysmeliahand deformity:Lowerhip:knee:Genu valgum · Genu varum · Genu recurvatum · Discoid meniscus · Congenital patellar dislocation · Congenital knee dislocationfoot deformity:Either / bothdactyly / digit:reduction deficits / limb:multiple joints:Axial CraniofacialCraniofacial dysostosis:other:spinal curvature (Scoliosis) · Klippel-Feil syndrome · Spondylolisthesis · Spina bifida occulta · SacralizationThoracic skeletonribs:sternum:M: JNT
anat(h/c, u, t, l)/phys
noco(arth/defr/back/soft)/cong, sysi/epon, injr
proc, drug(M01C, M4)
Congenital abnormality · multiple abnormalities (Q87, 759.7) Craniofacial Short stature 1q21.1 deletion syndrome · Aarskog–Scott syndrome · Cockayne syndrome · Cornelia de Lange Syndrome · Dubowitz syndrome · Noonan syndrome · Robinow syndrome · Silver–Russell syndrome · Seckel syndrome · Smith-Lemli-Opitz syndrome-Turner syndromeLimbs Overgrowth Laurence-Moon-Bardet-Biedl Bardet–Biedl syndrome · Laurence-Moon syndromeCombined/other,
known locus3 (Zimmerman-Laband syndrome) · 4/13 (Fraser syndrome) · 8 (Branchio-oto-renal syndrome) · 12 (Keutel syndrome, Timothy syndrome) · 15 (Marfan syndrome) · 19 (Donohue syndrome)Categories:- Medicine stubs
- Congenital disorders of musculoskeletal system
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