Gonzaga Amanda Katarinny Goes, Costa Carla Samily de Oliveira, Morais Hannah Gil de Farias, da Fonseca Neto Braz, Pinto Leão Pereira, Dantas Wagner Ranier Maciel, de Oliveira Patricia Teixeira, de Melo Daniela Pita
Postgraduate Program in Dental Sciences, Department of Dentistry, Federal University of Rio Grande do Norte, Natal, Brazil.
Graduate Program in Dentistry, Department of Dentistry, State University of Paraíba, Campina Grande, PB, Brazil.
Imaging Sci Dent. 2024 Mar;54(1):13-24. doi: 10.5624/isd.20230191. Epub 2024 Jan 4.
Pycnodysostosis (PYCD), an autosomal recessive syndrome, is characterized by an imbalance in bone remodeling that produces various clinical and radiographic craniofacial manifestations. This review represents a systematic examination of these manifestations, as well as oral features associated with PYCD.
A systematic review was conducted across 8 databases from February to March 2023. The search strategy focused on studies reporting cases of PYCD that examined the clinical and radiographic craniofacial and oral characteristics associated with this syndrome.
The review included 84 studies, encompassing a total of 179 cases of PYCD. More than half of the patients were female (55.3%), and the mean age was 14.7 years. Parental consanguinity was reported in 51.4% of the cases. The most common craniofacial clinical manifestation was a prominent nose, observed in 57.5% of cases. Radiographically, the most frequently reported craniofacial characteristics included the presence of an obtuse mandibular angle (84.3%) and frontal cranial bosses (82.1%). Clinical and radiographic examinations revealed oral alterations, with micrognathia present in 62.6% of patients and malocclusion in 59.2%. Among dental anomalies, tooth agenesis was the most commonly reported, affecting 15.6% of patients.
Understanding the clinical and radiographic craniofacial features of PYCD is crucial for dental professionals. This knowledge enables these clinicians to devise effective treatment plans and improve patient quality of life.
致密性成骨不全症(PYCD)是一种常染色体隐性综合征,其特征是骨重塑失衡,产生各种临床和影像学颅面部表现。本综述对这些表现以及与致密性成骨不全症相关的口腔特征进行了系统研究。
2023年2月至3月,在8个数据库中进行了系统综述。检索策略集中于报告致密性成骨不全症病例的研究,这些研究调查了与该综合征相关的临床和影像学颅面部及口腔特征。
该综述纳入了84项研究,共179例致密性成骨不全症病例。超过一半的患者为女性(55.3%),平均年龄为14.7岁。51.4%的病例报告有近亲结婚。最常见的颅面部临床表现是鼻子突出,57.5%的病例有此表现。在影像学上,最常报告的颅面部特征包括下颌角钝圆(84.3%)和额骨隆突(82.1%)。临床和影像学检查发现有口腔改变,62.6%的患者有小颌畸形,59.2%的患者有咬合不正。在牙齿异常中,最常报告的是牙齿缺失,影响了15.6%的患者。
了解致密性成骨不全症的临床和影像学颅面部特征对牙科专业人员至关重要。这些知识使临床医生能够制定有效的治疗方案并提高患者生活质量。