2014
DOI: 10.1016/j.jcms.2014.09.003
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Combination of Tessier clefts 3 and 4: Case report of a rare anomaly with 12 years' follow-up

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Cited by 12 publications
(5 citation statements)
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“…Four of the six FC 4 clefts had FC 7, FC 8, FC 9, and FC 10 clefts in association to their clefts while one presented with amniotic bands in the limbs as well (Table 3). Of the 16 articles that made the review, 4 (25%) reported associated clefts in 8 (28.6%) of the patients (Allam et al, 2014; Maeda et al, 2014; Golinko et al, 2018; Oh and Park, 2018). The FC 4 studies had no associated clefts reported but the FC 3 studies had 4 (14.3%) patients with FC 11 and 3 (10.7%) patients with FC 10 and 1 (3.6%) patient with FC 13 (Table 2).…”
Section: Resultsmentioning
confidence: 99%
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“…Four of the six FC 4 clefts had FC 7, FC 8, FC 9, and FC 10 clefts in association to their clefts while one presented with amniotic bands in the limbs as well (Table 3). Of the 16 articles that made the review, 4 (25%) reported associated clefts in 8 (28.6%) of the patients (Allam et al, 2014; Maeda et al, 2014; Golinko et al, 2018; Oh and Park, 2018). The FC 4 studies had no associated clefts reported but the FC 3 studies had 4 (14.3%) patients with FC 11 and 3 (10.7%) patients with FC 10 and 1 (3.6%) patient with FC 13 (Table 2).…”
Section: Resultsmentioning
confidence: 99%
“…The initial literature search yielded 35 articles with relevance to our study. After going through the title, abstract and full article screening, 16 articles (Gawrych et al, 2010; Laure et al, 2010; Sesenna et al, 2012; Wu et al, 2013; Allam et al, 2014; Bordoloi, 2014; Maeda et al, 2014; Spolyar et al, 2015; Mohammad Nor et al, 2016; Xu et al, 2016; Balaji, 2017; Assouan et al, 2018; Golinko et al, 2018; Oh and Park, 2018; Kim et al, 2019; Abdulwahab et al, 2020) were procured and enrolled for review (Table 2). Twelve (75%) of the articles originated from high-income countries while 4 (25%) were from low-income countries.…”
Section: Resultsmentioning
confidence: 99%
“…The management of patients with these rare craniofacial clefts is challenging and will require multidisciplinary team approach which will execute the care plan in an individualized, multistage treatment protocol (Versnel et al , 2011; Maeda et al , 2014). A suggested management protocol include: a detailed clinical evaluation, the use of 3D diagnostic imaging like the Computerized Tomographic Scan (CT) and Cone Beam Computerized Tomographic (CBCT) to delineate the full spectrum of the anomaly which ensure proper diagnosis.…”
Section: Introductionmentioning
confidence: 99%
“…Determination of ideal individualized upper arch form can be a valuable clinical guideline, particularly in patients with congenital anomalies and dentofacial deformities with malformed arch forms, such as those who need maxillary surgical reconstruction and parts of the maxilla is missing, due to accidents or facial clefts, or patients with a very underdeveloped maxilla [10]. In orthognathic patients, arch coordination is perceived as the major goal of presurgical orthodontic phase, which can be evaluated mainly by impression and stage recording in several clinical appointments, and any guide to facilitate these adaptations can be considered a significant step toward better clinical services.…”
Section: Introductionmentioning
confidence: 99%