2017
DOI: 10.1259/dmfr.20170154
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Three-dimensional imaging of soft and hard facial tissues in patients with craniofacial syndromes: a systematic review of methodological quality

Abstract: The median MINORS scores were only 50 and 54% of the maximum scores and there was a lack of prospective, controlled trials with sufficiently large study groups. To improve the quality of future studies in this domain and given the low incidence of craniofacial syndromes, more prospective multicentre controlled trials should be set up.

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Cited by 4 publications
(3 citation statements)
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“…Craniofacial malformations caused by synostoses and pharyngeal arch syndromes are less common, but can lead to severe proportional disfigurements of the head and face, including asymmetries. The extent of malformation and asymmetry can vary widely and affect both hard and soft facial tissues [92]. Examples are Treacher Collins, Crouzon, Apert, Pfeiffer and Saethre-Chotzen syndrome [93][94][95].…”
Section: Congenital Structural Asymmetries Of the Facementioning
confidence: 99%
“…Craniofacial malformations caused by synostoses and pharyngeal arch syndromes are less common, but can lead to severe proportional disfigurements of the head and face, including asymmetries. The extent of malformation and asymmetry can vary widely and affect both hard and soft facial tissues [92]. Examples are Treacher Collins, Crouzon, Apert, Pfeiffer and Saethre-Chotzen syndrome [93][94][95].…”
Section: Congenital Structural Asymmetries Of the Facementioning
confidence: 99%
“…On the one hand, there are many congenital, genetic disorders and multiple anomalies that interfere with bone development in the area of the skull and maxillary bones, which are encompassed under the collective term "craniofacial syndromes". They are directly associated with the development of bone and cartilage, affecting the form and function of the head and face [17], and include those associated with the oral cavity too.…”
Section: Cranio-maxillary Tissue Engineeringmentioning
confidence: 99%
“…The craniofacial syndromes can be considered as a collective term for a wide group of congenital, genetic disorders with multiple anomalies and major symptoms in the craniofacial area. They are directly associated with the development of bone and cartilage, affecting the form and function of the head and face [17] and include those associated with the oral cavity and face area such as cleft/lip palate (Moreau et al 2007; Martín-del-Campo, Rosales-Ibañez, y Rojo 2019). These orofacial cleft conditions have been estimated to have a global annual prevalence of 7.94 cases per 10,000 live births with high variances of treated patients across regions and countries causing a high economic impact worldwide [1, [20][21][22].…”
Section: Cranio-maxillary Tissue Engineeringmentioning
confidence: 99%