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Quoted phrase not found in phrase index: "Hypoplasia of maxilla relative to mandible"
Page 1
Binder syndrome.
Chummun S, McLean NR, Nugent M, Anderson PJ, David DJ. Chummun S, et al. J Craniofac Surg. 2012 Jul;23(4):986-90. doi: 10.1097/SCS.0b013e31824e2683. J Craniofac Surg. 2012. PMID: 22777437
Forty were males, and 32 were females, with an age range of 6 months to 47 years. Thirteen patients (18%) had a strong family history, and 65 patients (90%) have so far undergone surgical correction, and of those, 35 (54%) have completed their treatment, the longest follow …
Forty were males, and 32 were females, with an age range of 6 months to 47 years. Thirteen patients (18%) had a strong family history …
Crouzonodermoskeletal syndrome.
Jeftha A, Stephen L, Morkel JA, Beighton P. Jeftha A, et al. J Clin Pediatr Dent. 2004 Winter;28(2):173-6. doi: 10.17796/jcpd.28.2.72m01l5g50448548. J Clin Pediatr Dent. 2004. PMID: 14969379 Free article.
Radiographic examination conducted shortly after birth revealed the presence of several tooth buds in both the maxillae and the mandible. The delayed eruption of the teeth will be of significance in future orthodontic and maxillofacial measures for the improvement o …
Radiographic examination conducted shortly after birth revealed the presence of several tooth buds in both the maxillae and the ma …
SH3BP2-related fibro-osseous disorders of the maxilla and mandible: A systematic review.
Kueper J, Tsimbal C, Olsen BR, Kaban L, Liao EC. Kueper J, et al. Int J Oral Maxillofac Surg. 2022 Jan;51(1):54-61. doi: 10.1016/j.ijom.2021.04.001. Epub 2021 Apr 30. Int J Oral Maxillofac Surg. 2022. PMID: 33941395 Review.
Thirty publications were identified, including 92 individuals from 34 families, who were diagnosed with SH3BP2-related fibro-osseous lesions of the jaw. Only 15% of cases included in this review had no known family history of the disease. The distribution of cherubism was …
Thirty publications were identified, including 92 individuals from 34 families, who were diagnosed with SH3BP2-related fibro-osseous lesions …
Molecular Basis for Craniofacial Phenotypes Caused by Sclerostin Deletion.
Chen J, Yuan X, Pilawski I, Liu X, Delgado-Calle J, Bellido T, Turkkahraman H, Helms JA. Chen J, et al. J Dent Res. 2021 Mar;100(3):310-317. doi: 10.1177/0022034520963584. Epub 2020 Oct 20. J Dent Res. 2021. PMID: 33078679 Free PMC article.
Affected patients have a high bone mass coupled with a distinctive appearance where the mandible is enlarged and the maxilla is foreshortened. Here, mice carrying a null mutation in Sost were analyzed using quantitative micro-computed tomographic (CT) imaging and hi …
Affected patients have a high bone mass coupled with a distinctive appearance where the mandible is enlarged and the maxilla i …
Prevalence and Distribution of Dental Anomalies in Schoolchildren in Kuwait.
Alanzi A, Bufersen N, Haider S, Abdulrahim M. Alanzi A, et al. Int Dent J. 2024 Jun;74(3):566-572. doi: 10.1016/j.identj.2023.10.019. Epub 2024 Jan 29. Int Dent J. 2024. PMID: 38290916 Free PMC article.
The most prevalent anomaly was dental agenesis (9.3%), followed by taurodontism (6.6%) and ectopic eruption (EE, 2%). DA were more common in the maxilla (58.2%) compared to the mandible (41.8%, P = .042). Congenitally missing teeth were significantly more frequent i …
The most prevalent anomaly was dental agenesis (9.3%), followed by taurodontism (6.6%) and ectopic eruption (EE, 2%). DA were more common in …
Loeys-Dietz and Shprintzen-Goldberg syndromes: analysis of TGF-β-opathies with craniofacial manifestations using an innovative multimodality method.
Almpani K, Liberton DK, Jani P, Keyvanfar C, Mishra R, Curry N, Orzechowski P, Frischmeyer-Guerrerio PA, Lee JS. Almpani K, et al. J Med Genet. 2022 Oct;59(10):938-946. doi: 10.1136/jmedgenet-2021-107695. Epub 2021 Dec 16. J Med Genet. 2022. PMID: 34916229 Free PMC article.
RESULTS: The most common craniofacial features detected in this cohort include mandibular retrognathism (84%), flat midface projection (84%), abnormal eye shape (73%), low-set ears (73%), abnormal nose (66%) and lip shape (64%), hypertelorism (41%) and a relatively high pr …
RESULTS: The most common craniofacial features detected in this cohort include mandibular retrognathism (84%), flat midface projection (84%) …
Calcifying epithelial odontogenic tumour: biological profile based on 181 cases from the literature.
Philipsen HP, Reichart PA. Philipsen HP, et al. Oral Oncol. 2000 Jan;36(1):17-26. doi: 10.1016/s1368-8375(99)00061-5. Oral Oncol. 2000. PMID: 10889914 Review.
Both variants have an almost 1:1 gender ratio. The intraosseous CEOT shows a maxilla:mandible site ratio of 1:2 and are mainly located in the premolar/molar region. ...Histological variants including CEOT with cementum-like components, clear-cell CEOT (15 cases repo …
Both variants have an almost 1:1 gender ratio. The intraosseous CEOT shows a maxilla:mandible site ratio of 1:2 and are mainly …
Treacher Collins syndrome: A novel TCOF1 mutation and monopodial stapes.
Kantaputra PN, Tripuwabhrut K, Intachai W, Carlson BM, Quarto N, Ngamphiw C, Tongsima S, Sonsuwan N. Kantaputra PN, et al. Clin Otolaryngol. 2020 Sep;45(5):695-702. doi: 10.1111/coa.13560. Epub 2020 May 25. Clin Otolaryngol. 2020. PMID: 32351010 Free article.
OBJECTIVE: To investigate four Treacher Collins syndrome patients of the Sgaw Karen family living in Thailand. METHOD: Clinical examination, hearing tests, lateral cephalometric analyses, Computed tomography, whole exome sequencing and Sanger direct sequencing were perform …
OBJECTIVE: To investigate four Treacher Collins syndrome patients of the Sgaw Karen family living in Thailand. METHOD: Clinical exami …
Vertical facial skeletal dysplasias: the oral surgical connection.
Rimer S. Rimer S. Compend Contin Educ Dent. 1997 Dec;18(12):1198-200, 1202-4, 1206-7 passim. Compend Contin Educ Dent. 1997. PMID: 9656844 Review.
Oral surgery can open new vistas of treatment for patients with vertical abnormalities of the face, jaw, and teeth. An interdisciplinary approach is critical, however, incorporating the insights and skills of restorative, orthodontic, periodontal and surgical practitioners …
Oral surgery can open new vistas of treatment for patients with vertical abnormalities of the face, jaw, and teeth. An interdisciplin …
Clinical and Molecular Study of ELMO-2-Related Massive Intraosseous Vascular Malformations: Lessons Learned From 25 Years of Follow-up.
Vargel I, Calis M, Canter HI, Cil BE. Vargel I, et al. Ann Plast Surg. 2019 Sep;83(3):293-299. doi: 10.1097/SAP.0000000000001786. Ann Plast Surg. 2019. PMID: 30882408
Massive intraosseous vascular malformations, a relatively rare entity in the vascular malformation spectrum, deserves attention as involving the membranous bones of the craniofacial skeleton and may lead to severe life-threatening hemorrhages and even death. ...All the pat …
Massive intraosseous vascular malformations, a relatively rare entity in the vascular malformation spectrum, deserves attention as in …
34 results