Upper cervical spine and craniofacial morphology in hypohidrotic ectodermal dysplasia

被引:8
作者
Sonnesen L. [1 ]
Jasemi A. [1 ]
Gjørup H. [2 ]
Daugaard-Jensen J. [3 ]
机构
[1] Orthodontics, Department of Odontology, Faculty of Health and Medical Sciences, University of Copenhagen, 20 Nørre Allé, Copenhagen N
[2] Centre for Oral Health in Rare Diseases, Department of Maxillofacial Surgery, University Hospital, Nørrebrogade 44, Aarhus C
[3] Centre for Oral Health in Rare Diseases, University Hospital of Copenhagen, Blegdamsvej 9, Copenhagen Ø
关键词
Cervical vertebrae; Child; Craniofacial abnormalities; Hypohidrotic ectodermal dysplasia; Notochord; Spinal column;
D O I
10.1007/s40368-018-0362-8
中图分类号
学科分类号
摘要
Aim: 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. Methods: 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. Results: 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). Conclusions: 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. © 2018, European Academy of Paediatric Dentistry.
引用
收藏
页码:331 / 336
页数:5
相关论文
共 50 条
  • [21] Hypohidrotic Ectodermal Dysplasia: A Rare Disorder With Bilateral Infantile Glaucoma
    Dubey, Suneeta
    Bhoot, Madhu
    Jain, Kanika
    JOURNAL OF GLAUCOMA, 2019, 28 (04) : E58 - E60
  • [22] Characterization of EDARADD gene mutations responsible for hypohidrotic ectodermal dysplasia
    Asano, Nobuyuki
    Yasuno, Shuichiro
    Hayashi, Ryota
    Shimomura, Yutaka
    JOURNAL OF DERMATOLOGY, 2021, 48 (10) : 1533 - 1541
  • [23] Quantification of taurodontism: interests in the early diagnosis of hypohidrotic ectodermal dysplasia
    Gros, C-I
    Clauss, F.
    Obry, F.
    Maniere, M. C.
    Schmittbuhl, M.
    ORAL DISEASES, 2010, 16 (03) : 292 - 298
  • [24] Prosthetic Rehabilitation in Patients with Hypohidrotic Ectodermal Dysplasia: Clinical Case
    Torres Leon, Blanca Liliana
    Martins, Gabriela Botelho
    Meyer, Guilherme Andrade
    dos Santos, Manuela Serra
    Cesar, Yelena Araujo
    REVISTA PORTUGUESA DE ESTOMATOLOGIA MEDICINA DENTARIA E CIRURGIA MAXILOFACIAL, 2008, 49 (03): : 153 - 158
  • [25] A case of multiple oral cancers in the patient with hypohidrotic ectodermal dysplasia
    Kobayashi, Takanori
    Iida, Akihiko
    Narimatsu, Kaya
    Shimomura, Yutaka
    JOURNAL OF ORAL AND MAXILLOFACIAL SURGERY MEDICINE AND PATHOLOGY, 2022, 34 (06) : 759 - 763
  • [26] Masticatory function in growing individuals with hypohidrotic ectodermal dysplasia: A longitudinal study
    Ding, Meili
    Kang, Yanfeng
    Qin, Man
    Zhu, Junxia
    INTERNATIONAL JOURNAL OF PAEDIATRIC DENTISTRY, 2024,
  • [27] Clinical and molecular study in a family with autosomal dominant hypohidrotic ectodermal dysplasia
    Callea, Michele
    Cammarata-Scalisi, Francisco
    Willoughby, Colin E.
    Giglio, Sabrina R.
    Sani, Ilaria
    Bargiacchi, Sara
    Traficante, Giovanna
    Bellacchio, Emanuele
    Tadini, Gianluca
    Yavuz, Izzet
    Galeotti, Angela
    Clarich, Gabriella
    ARCHIVOS ARGENTINOS DE PEDIATRIA, 2017, 115 (01): : E34 - E38
  • [28] Hypohidrotic (Anhidrotic) ectodermal dysplasia - a rare cause of childhood Atrophic Rhinitis
    Dasgupta K.S.
    Joshi S.V.
    Gawarle S.H.
    Murkey N.S.N.
    Avad A.
    Indian Journal of Otolaryngology and Head and Neck Surgery, 2006, 58 (2) : 202 - 204
  • [29] Treatment with removable prosthesis in hypohidrotic ectodermal dysplasia.: A clinical case
    Pipa Vallejo, Adolfo
    Lopez-Arranz Monje, Elena
    Gonzalez Garcia, Manuel
    Martinez Fernandez, Miguel
    Blanco-Moreno Alvarez-Buylla, Fernando
    MEDICINA ORAL PATOLOGIA ORAL Y CIRUGIA BUCAL, 2008, 13 (02): : E119 - E123
  • [30] Mutations in EDARADD account for a small proportion of hypohidrotic ectodermal dysplasia cases
    Chassaing, N.
    Cluzeau, C.
    Bal, E.
    Guigue, P.
    Vincent, M-C
    Viot, G.
    Ginisty, D.
    Munnich, A.
    Smahi, A.
    Calvas, P.
    BRITISH JOURNAL OF DERMATOLOGY, 2010, 162 (05) : 1044 - 1048