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Quoted phrase not found in phrase index: "Abnormal morphology of bony orbit of skull"
Page 1
Management of the Airway in Apert Syndrome.
Xie C, De S, Selby A. Xie C, et al. J Craniofac Surg. 2016 Jan;27(1):137-41. doi: 10.1097/SCS.0000000000002333. J Craniofac Surg. 2016. PMID: 26674912
This rare syndrome, occurring in up to approximately 1 in 65,000 live births, results in airway compromise at various anatomic levels, in addition to abnormal central respiratory drive. Obstructive apneas arise because of decreased airway caliber, which may occur in the fo …
This rare syndrome, occurring in up to approximately 1 in 65,000 live births, results in airway compromise at various anatomic levels, in ad …
Periorbital lymphatic malformation: clinical course and management in 42 patients.
Greene AK, Burrows PE, Smith L, Mulliken JB. Greene AK, et al. Plast Reconstr Surg. 2005 Jan;115(1):22-30. Plast Reconstr Surg. 2005. PMID: 15622227 Review.
Ocular proptosis was temporarily managed by tarsorrhaphy (n = 9), but expansion of the bony orbit was needed to correct persistent proptosis (n = 8). Orbital exenteration was necessary in two patients....
Ocular proptosis was temporarily managed by tarsorrhaphy (n = 9), but expansion of the bony orbit was needed to correct persis …
Cephalometric analysis of craniofacial morphology and growth in unrepaired isolated cleft palate patients.
Xu Y, Yang C, Schreuder WH, Shi J, Shi B, Zheng Q, Wang Y. Xu Y, et al. J Craniomaxillofac Surg. 2014 Dec;42(8):1853-60. doi: 10.1016/j.jcms.2014.07.003. Epub 2014 Jul 29. J Craniomaxillofac Surg. 2014. PMID: 25169446
RESULTS: UICP patients in childhood showed a shortened cranial basal length; reduced bony nasopharyngeal height; short maxillary depth and height with a posterior positioned maxilla and an increased width of the nasal cavity, maxilla and orbit; and a shortened mandi …
RESULTS: UICP patients in childhood showed a shortened cranial basal length; reduced bony nasopharyngeal height; short maxillary dept …
On the origin of bitemporal hollowing.
van der Meulen JJ, Willemsen J, van der Vlugt J, Nazir PR, Hilling D, Mathijssen IM, Ongkosuwito E, van Adrichem LN, Vaandrager MJ, Hovius SE; Dutch Craniofacial Unit. van der Meulen JJ, et al. J Craniofac Surg. 2009 May;20(3):752-6. doi: 10.1097/SCS.0b013e3181a2e44a. J Craniofac Surg. 2009. PMID: 19381101
RESULTS: A significant relation was found between a severe deformation seen at postoperative photographic evaluation and a lower growth ratio. The preoperative photo score was not of predicting value for the postoperative growth ratio and therefore, indirectly, for the pos …
RESULTS: A significant relation was found between a severe deformation seen at postoperative photographic evaluation and a lower growth rati …
Innovative Surgical Treatment of Severe Cherubism.
Son JH, Marshall DC, Valiathan M, Otteson T, Ferretti G, Grigorian PA, Rosen C, Becker D, Rowe D, Soltanian H, Lakin G. Son JH, et al. Cleft Palate Craniofac J. 2019 Jan;56(1):90-93. doi: 10.1177/1055665618774008. Epub 2018 May 22. Cleft Palate Craniofac J. 2019. PMID: 29787301
BACKGROUND: Cherubism is an autosomal dominant syndrome characterized by excessive bilateral maxillomandibular bony degeneration and fibrous tissue hyperplasia. Conservative management is the preferred treatment as cherubism has a self-limiting course. ...
BACKGROUND: Cherubism is an autosomal dominant syndrome characterized by excessive bilateral maxillomandibular bony degeneration and …
Congenital Ocular Dystopia from Orbitofrontal Bone Dysplasia.
Swanson JW, Bartlett SP. Swanson JW, et al. Plast Reconstr Surg. 2016 Jan;137(1):125e-134e. doi: 10.1097/PRS.0000000000001922. Plast Reconstr Surg. 2016. PMID: 26710043
The features and treatment of these patients were analyzed. RESULTS: Four patients with congenital orbitofrontal bone dysplasia were identified, three with unilateral and one with bilateral frontal bone defects. Clinical signs of hypoglobus and vertical ocular dystopia of …
The features and treatment of these patients were analyzed. RESULTS: Four patients with congenital orbitofrontal bone dysplasia were …
Blood within the bone: orbital intraosseous venous malformation.
Bhattacharjee K, Rehman O, Venkatraman V, Das D, Mohapatra SSD, Gogoi R, Soni D. Bhattacharjee K, et al. Orbit. 2024 Jun;43(3):316-328. doi: 10.1080/01676830.2024.2303761. Epub 2024 Jan 23. Orbit. 2024. PMID: 38261337 Review.
Histopathology revealed vascular spaces with endothelial lining, separated by bony trabeculae in all patients. Follow-up periods ranged from 6 to 48 months and no recurrence or progression were noted. CONCLUSIONS: OIVM is an exceptionally rare disorder with a gradually pro …
Histopathology revealed vascular spaces with endothelial lining, separated by bony trabeculae in all patients. Follow-up periods rang …
Orbital Dysmorphology in Untreated Children with Crouzon and Apert Syndromes.
Forte AJ, Steinbacher DM, Persing JA, Brooks ED, Andrew TW, Alonso N. Forte AJ, et al. Plast Reconstr Surg. 2015 Nov;136(5):1054-1062. doi: 10.1097/PRS.0000000000001693. Plast Reconstr Surg. 2015. PMID: 26505706

The mean age of the Apert group was 5.31 5 years; Crouzon, 5.77 2.7 years; and control, 6.4 3.6 years. The bony orbit length was 12 percent shorter in Apert (p = 0.004) and 17 percent shorter in the Crouzon group when compared to controls (p < 0.0001). ...Despite

The mean age of the Apert group was 5.31 5 years; Crouzon, 5.77 2.7 years; and control, 6.4 3.6 years. The bony orbit length w …
Computer-assisted midface reconstruction in Treacher Collins syndrome part 1: skeletal reconstruction.
Herlin C, Doucet JC, Bigorre M, Khelifa HC, Captier G. Herlin C, et al. J Craniomaxillofac Surg. 2013 Oct;41(7):670-5. doi: 10.1016/j.jcms.2013.01.007. Epub 2013 Mar 1. J Craniomaxillofac Surg. 2013. PMID: 23454266
The palate as well as the external and middle ear are also affected, but his prognosis is mainly related to neonatal airway management. Methods of zygomatico-orbital reconstruction are numerous and currently use primarily autologous bone, lyophilized cartilage, alloplastic …
The palate as well as the external and middle ear are also affected, but his prognosis is mainly related to neonatal airway managemen …
Ocular refractive and biometric characteristics in patients with thalassaemia major.
Nowroozzadeh MH, Kalantari Z, Namvar K, Meshkibaf MH. Nowroozzadeh MH, et al. Clin Exp Optom. 2011 Jul;94(4):361-6. doi: 10.1111/j.1444-0938.2010.00579.x. Epub 2011 Feb 16. Clin Exp Optom. 2011. PMID: 21323733 Free article.
BACKGROUND: Thalassaemia major is associated with characteristic findings in craniofacial bony structures and thereby may render abnormal bony orbit and subsequently distinctive ocular biometry. ...
BACKGROUND: Thalassaemia major is associated with characteristic findings in craniofacial bony structures and thereby may render a
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