Villeneuve d'ascq Pivate hospital, Villeneuve-d'Ascq.
Department of Oral and Maxillofacial Surgery, University Lille, CHU Lille, INSERM U 1008, Controlled Drug Delivery Systems and Biomaterials.
J Craniofac Surg. 2021;32(8):2823-2826. doi: 10.1097/SCS.0000000000007707.
Otopalatodigital syndrome spectrum disorders are caused by Filamin A (FLNA) gene mutations. Otopalatodigital syndrome spectrum disorders are a group of rare congenital skeletal dysplasia, with specific craniomaxillofacial features including otopalatodigital syndrome type 1 and type 2, Melnick-Needles syndrome, frontometaphyseal dysplasia, terminal osseous dysplasia with pigmentary defects. The authors describe cases of a young girl with Melnick-Needles syndrome and a young boy with frontometaphyseal dysplasia treated in the Oral and Maxillofacial Surgery Department. Both patients had FLNA gene mutation confirmed with molecular genetic analysis. The authors proposed a 4 step treatment of the malformations with good outcomes both aesthetically and functionally, without complication.
眼-腭-指(趾)综合征谱疾病是由细丝蛋白 A (FLNA)基因突变引起的。眼-腭-指(趾)综合征谱疾病是一组罕见的先天性骨骼发育不良,具有特定的颅面特征,包括 1 型和 2 型眼-腭-指(趾)综合征、Melnick-Needles 综合征、额骨-筛骨发育不良、伴色素缺陷的末端骨发育不良。作者描述了在口腔颌面外科治疗的患有 Melnick-Needles 综合征的年轻女孩和患有额骨-筛骨发育不良的年轻男孩的病例。两名患者均通过分子遗传学分析证实存在 FLNA 基因突变。作者提出了一种 4 步治疗方案,对畸形进行治疗,在美学和功能上均取得了良好的效果,且无并发症。