Sonnesen L, Jasemi A, Gjørup H, Daugaard-Jensen J
Orthodontics, Department of Odontology, Faculty of Health and Medical Sciences, University of Copenhagen, 20 Nørre Allé, 2200, Copenhagen N, Denmark.
Centre for Oral Health in Rare Diseases, Department of Maxillofacial Surgery, University Hospital, Nørrebrogade 44, 8000, Aarhus C, Denmark.
Eur Arch Paediatr Dent. 2018 Oct;19(5):331-336. doi: 10.1007/s40368-018-0362-8. Epub 2018 Aug 20.
Morphological deviations in the upper cervical spine and craniofacial morphology in patients with X-linked hypohidrotic ectodermal dysplasia (XLHED) were compared to non-syndromic controls.
All children and adolescents with genetically verified XLHED, registered at the Resource Centres for Oral Health in Rare Diseases, who met the inclusion criteria, were included. The group thus comprised 15 XLHED patients (3 girls and 12 boys, aged 8-16 years, mean 11.2 years). The control group comprised 22 non-syndromic pre-orthodontic children (14 girls and 8 boys aged 9-16 years, mean 11.9 years) with agenesis of one tooth, neutral occlusion and normal craniofacial morphology. The craniofacial and upper spine morphology was analysed on lateral cephalograms by standard methods. Differences between XLHED patients and controls were tested and adjusted for age and gender by multiple regression analyses.
Morphological deviations in the upper spine occur significantly more often in XLHED patients compared to controls (60 vs. 9.1%; p < 0.01). The cranial base angle (n-s-ar, p < 0.05), sagittal jaw relationship (ss-n-pg, p < 0.001), maxillary inclination (NSL/NL, p < 0.001) and mandibular inclination (NSL/ML, p < 0.01) were significantly smaller in XLHED patients compared to controls. The mandibular prognathia (s-n-pg) was significantly larger in XLHED patients compared to controls (p < 0.05).
The upper spine and the craniofacial morphology were different in XLHED patients compared to controls. The results of this study may contribute to a further understanding of the craniofacial and spinal phenotypic spectrum in patients with XLHED and thus have implications for diagnosis and treatment planning of these patients.
将X连锁隐性遗传性外胚层发育不良(XLHED)患者的上颈椎形态学偏差和颅面形态与非综合征性对照进行比较。
纳入所有在罕见病口腔健康资源中心登记的、基因检测证实为XLHED且符合纳入标准的儿童和青少年。该组包括15例XLHED患者(3名女孩和12名男孩,年龄8 - 16岁,平均11.2岁)。对照组包括22名非综合征性正畸前儿童(14名女孩和8名男孩,年龄9 - 16岁,平均11.9岁),有一颗牙齿缺失,中性咬合,颅面形态正常。通过标准方法在头颅侧位片上分析颅面和上脊柱形态。通过多元回归分析测试XLHED患者与对照组之间的差异,并对年龄和性别进行调整。
与对照组相比,XLHED患者上脊柱形态偏差的发生率显著更高(60%对9.1%;p < 0.01)。与对照组相比,XLHED患者的颅底角(n - s - ar,p < 0.05)、矢状颌关系(ss - n - pg,p < 0.001)、上颌倾斜度(NSL/NL,p < 0.001)和下颌倾斜度(NSL/ML,p < 0.01)显著更小。与对照组相比,XLHED患者的下颌前突(s - n - pg)显著更大(p < 0.05)。
与对照组相比,XLHED患者的上脊柱和颅面形态不同。本研究结果可能有助于进一步了解XLHED患者的颅面和脊柱表型谱,从而对这些患者的诊断和治疗计划具有指导意义。