Application advances of imaging and three-dimensional digital technology for an early diagnosis of Pierre Robin syndrome

References:

[1] Baxter D, Shanks AL.Pierre Robin syndrome[M/OL]//Anon.StatPearls[Internet].Treasure Island:StatPearls Publishing, 2022:NBK562213.https://pubmed.ncbi.nlm.nih.gov/32965884/.
[2] Varadarajan S, Balaji TM, Raj AT, et al.Genetic mutations associated with Pierre Robin syndrome/sequence:a systematic review[J].Mol Syndromol, 2021, 12(2):69-86.DOI:10.1159/000513217.
[3] Cole A, Lynch P, Slator R.A new grading of Pierre Robin sequence[J].Cleft Palate Craniofac J, 2008, 45(6):603-606.DOI:10.1597/07-129.1.
[4] Sahoo NK, Roy ID, Dalal S, et al.Distraction osteogenesis for management of severe OSA in Pierre Robin sequence:an approach to elude tracheostomy in infants[J].J Maxillofac Oral Surg, 2016, 15(4):501-505.DOI:10.1007/s12663-016-0888-4.
[5] Shen WM, Jie C, Chen JB, et al.Mandibular distraction osteogenesis to relieve Pierre Robin severe airway obstruction in neonates:indication and operation[J].J Craniofac Surg, 2009, 20(Suppl 2):1812-1816.DOI:10.1097/SCS.0b013e3181b6c388.
[6] Marsza?ek-Kruk BA, Wójcicki P, Dowgierd K, et al.Treacher Collins syndrome:genetics, clinical features and management[J].Genes (Basel), 2021, 12(9):1392.DOI:10.3390/genes12091392.
[7] 官勇, 李胜利, 陈琮瑛, 等.产前超声诊断Pierre Robin序列征[J].中华超声影像学杂志, 2020, 29(9):790-793.DOI:10.3760/cma.j.cn131148-20200421-00323. Guan Y, Li SL, Chen CY, et al.Prenatal ultrasonic diagnosis of Pierre Robin sequence[J].Chin J Ultrasonogr, 2020, 29(9):790-793.DOI:10.3760/cma.j.cn131148-20200421-00323.
[8] Luedders DW, Bohlmann MK, Germer U, et al.Fetal micrognathia:objective assessment and associated anomalies on prenatal sonogram[J].Prenat Diagn, 2011, 31(2):146-151.DOI:10.1002/pd.2661.
[9] 王丽敏, 马小燕, 江玮, 等.胎儿鼻后三角在妊娠早期筛查颜面部畸形中的应用价值[J].临床超声医学杂志, 2014, 16(6):369-372.DOI:10.16245/j.cnki.issn1008-6978.2014.06.004. Wang LM, Ma XY, Jiang W, et al.Application value of retronasal triangle in ultrasonic screening of fetal facial anomalies in first trimester[J].J Clin Ultrasound Med, 2014, 16(6):369-372.DOI:10.16245/j.cnki.issn1008-6978.2014.06.004.
[10] 徐巧阳, 董雪琴, 吴洁丽.三维超声产前诊断胎儿小下颌畸形的临床意义[J].中国优生与遗传杂志, 2016, 24(8):100-101, 55, 140.DOI:10.13404/j.cnki.cjbhh.2016.08.045. Xu QY, Dong XQ, Wu JL.Clinical significance of three-dimensional ultrasound in prenatal diagnosis of micrognathia[J].Chine J Birth Health Hered, 2016, 24(8):100-101, 55, 140.DOI:10.13404/j.cnki.cjbhh.2016.08.045.
[11] Bruce MK, Islam R, Anstadt EE, et al.Mandibular measurements at the 20-week anatomy ultrasound as a prenatal diagnostic predictor of Pierre Robin sequence[J].Cleft Palate Craniofac J, 2023, 60(3):352-358.DOI:10.1177/10556656211064771.
[12] Kruse T, Neuschulz J, Wilhelm L, et al.Prenatal diagnosis of Robin sequence:sensitivity, specificity, and clinical relevance of an index for micrognathia[J].Cleft Palate Craniofac J, 2021, 58(8):1012-1019.DOI:10.1177/1055665620972297.
[13] D’Ambrosio V, Vena F, Manganaro L, et al.Fetal tongue posture associated with micrognathia:an ultrasound marker of cleft secondary palate?[J].J Clin Ultrasound, 2020, 48(1):48-51.DOI:10.1002/jcu.22784.
[14] Ji Y, Cui J, Kong LL, et al.Significance of three-dimensional ultrasound screening of fetal micrognathia[J].J Plast Reconstr Aesthet Surg, 2022, 75(4):1497-1520.DOI:10.1016/j.bjps.2022.01.025.
[15] 高雅丽, 彭松, 杨巧丽.Pierre Robin序列征磁共振表现一例报道及文献复习[J].中国当代医药, 2021, 28(8):200-202.DOI:10.3969/j.issn.1674-4721.2021.08.057. Gao YL, Peng S, Yang QL.A case report and literature review of MRI manifestations of Pierre Robin sequence sign[J].China Mod Med, 2021, 28(8):200-202.DOI:10.3969/j.issn.1674-4721.2021.08.057.
[16] Rubio EI.Imaging of the fetal oral cavity, airway and neck[J].Pediatr Radiol, 2021, 51(7):1122-1133.DOI:10.1007/s00247-020-04851-6.
[17] Rogers-Vizena CR, Mulliken JB, Daniels KM, et al.Prenatal features predictive of Robin sequence identified by fetal magnetic resonance imaging[J].Plast Reconstr Surg, 2016, 137(6):999e-1006e.DOI:10.1097/PRS.0000000000002193.
[18] Toren A, Spevac S, Hoffman C, et al.What does the normal fetal face look like? MR imaging of the developing mandible and nasal cavity[J].Eur J Radiol, 2020, 126:108937.DOI:10.1016/j.ejrad.2020.108937.
[19] 丁楚涵, 边传振, 卞宠平."黑骨"MRI研究儿童颅缝早闭进展[J].中国医学影像技术, 2022, 38(8):1259-1261.DOI:10.13929/j.issn.1003-3289.2022.08.033. Ding CH, Bian CZ, Bian CP.Recent advances of "black bone" MRI in children with craniosynostosis[J].Chin J Med Imaging Technol, 2022, 38(8):1259-1261.DOI:10.13929/j.issn.1003-3289.2022.08.033.
[20] Lopes PML, Moreira CR, Perrella A, et al.3-D volume rendering maxillofacial analysis of angular measurements by multislice CT[J].Oral Surg Oral Med Oral Pathol Oral Radiol Endod, 2008, 105(2):224-230.DOI:10.1016/j.tripleo.2007.08.036.
[21] Vendittelli BL, Dec W, Warren SM, et al.The importance of vector selection in preoperative planning of bilateral mandibular distraction[J].Plast Reconstr Surg, 2008, 122(4):1144-1153.DOI:10.1097/PRS.0b013e318185d596.
[22] Humphries LS, Reid RR, Ross CF, et al.Biomechanical and morphological analysis of Pierre Robin sequence mandible:finite element and morphometric study[J].Anat Rec (Hoboken), 2021, 304(7):1375-1388.DOI:10.1002/ar.24543.
[23] 吴琼, 陈凤仪, 夏旋.基于CT三维头颅重建技术诊断Pierre Robin综合征1例[J].巴楚医学, 2018, 1(4):79-81.DOI:10.3969/j.issn.2096-6113.2018.04.017. Wu Q, Chen FY, Xia X.One case report of Pierre Robin syndrome diagnosed by three-dimensional reconstruction of skull based upon computed tomography (CT) scans[J].Bachu Med J, 2018, 1(4):79-81.DOI:10.3969/j.issn.2096-6113.2018.04.017.
[24] El Amm CA, Denny A.Hyoid bone abnormalities in Pierre Robin patients[J].J Craniofac Surg, 2008, 19(1):259-263.DOI:10.1097/scs.0b013e31815c9460.
[26] 李光荣, 郭斌, 张新荣.Pierre-Robin综合征的CT表现及分型[J].中国医学计算机成像杂志, 2014, 20(6):544-547.DOI:10.19627/j.cnki.cn31-1700/th.2014.06.016. Li GR, Guo B, Zhang XR.Imaging findings and classification of Pierre-Robin syndrome[J].Chin Comput Med Imaging, 2014, 20(6):544-547.DOI:10.19627/j.cnki.cn31-1700/th.2014.06.016.
[27] 朱丽哲.小下颌畸形患者下颌前徙术后上气道形态及气流动力学研究[D].西安:第四军医大学, 2015. Zhu LZ.Upper airway morphology and flow dynamics of patients with micrognathia after mandibular advancement[D].Xi’an:The Fourth Military Medical University, 2015.
[28] Duarte DW, Schweiger C, Manica D, et al.Predictors of respiratory dysfunction at diagnosis of Robin sequence[J].Laryngoscope, 2021, 131(12):2811-2816.DOI:10.1002/lary.29685.
[29] 施雄.锥形束CT低剂量扫描可行性和临床应用的初步研究[D].上海:中国人民解放军海军军医大学, 2020.DOI:10.26998/d.cnki.gjuyu.2020.000261. Shi X.Feasibility and clinical application of low-dose CBCT[D].Shanghai:Naval Medical University, 2020.DOI:10.26998/d.cnki.gjuyu.2020.000261.
[30] 车蓓, 顾月光, 马俊青, 等.下颌后缩患者上气道三维结构和舌骨位置的分析[J].南京医科大学学报(自然科学版), 2012, 32(4):532-535. Che B, Gu YG, Ma JQ, et al.Analysis of three dimensional upper airway structure and hyoid position in retrognathic patients[J].J Nanjing Med Univ (Nat Sci), 2012, 32(4):532-535.
[31] Yellon RF.Epiglottic and base-of-tongue prolapse in children:grading and management[J].Laryngoscope, 2006, 116(2):194-200.DOI:10.1097/01.mlg.0000191562.67363.e5.
[32] Ishman SL, Chang KW, Kennedy AA.Techniques for evaluation and management of tongue-base obstruction in pediatric obstructive sleep apnea[J].Curr Opin Otolaryngol Head Neck Surg, 2018, 26(6):409-416.DOI:10.1097/MOO.0000000000000489.
[33] Banhara FL, Trindade IEK, Trindade-Suedam IK, et al.Respiratory sleep disorders, nasal obstruction and enuresis in children with non-syndromic Pierre Robin sequence[J].Braz J Otorhinolaryngol, 2022, 88(Suppl 1):S133-S141.DOI:10.1016/j.bjorl.2021.05.002.
[34] Morrison KA, Collares MV, Flores RL.Robin sequence:neonatal mandibular distraction[J].Clin Plast Surg, 2021, 48(3):363-373.DOI:10.1016/j.cps.2021.03.005.