Lenormand Anaëlle, Khonsari Roman, Corre Pierre, Perrin Jean Philippe, Boscher Cécile, Nizon Mathilde, Pichon Olivier, David Albert, Le Caignec Cedric, Bertin Helios, Isidor Bertrand
Clinique de Stomatologie et de Chirurgie Maxillo-Faciale, CHU de Nantes, Nantes, France.
Assistantce publique-hôpitaux de Paris, Service de chirurgie maxillofaciale et plastique, Hôpital Universitaire Necker-Enfants Malades, Université Sorbonne Paris cité, Université Paris-Descartes, Paris, France.
Am J Med Genet A. 2018 Jul;176(7):1614-1617. doi: 10.1002/ajmg.a.38690. Epub 2018 Apr 28.
Ankyloglossia is a congenital oral anomaly characterized by the presence of a hypertrophic and short lingual frenulum. Mutations in the gene encoding the transcription factor TBX22 have been involved in isolated ankyloglossia and X-linked cleft palate. The knockout of Lgr5 in mice results in ankyloglossia. Here, we report a five-generation family including patients with severe ankyloglossia and missing lower central incisors. Two members of this family also exhibited congenital anorectal malformations. In this report, male-to-male transmission was in favor of an autosomal dominant inheritance, which allowed us to exclude the X-linked TBX22 gene. Linkage analysis using short tandem repeat markers located in the vicinity of LGR5 excluded this gene as a potential candidate. These results indicate genetic heterogeneity for ankyloglossia. Further investigations with additional families are required in order to identify novel candidate genes.
舌系带过短是一种先天性口腔异常,其特征是存在肥厚且短的舌系带。编码转录因子TBX22的基因突变与孤立性舌系带过短和X连锁腭裂有关。小鼠中Lgr5基因敲除会导致舌系带过短。在此,我们报告了一个五代家族,其中包括患有严重舌系带过短和下中切牙缺失的患者。该家族的两名成员还表现出先天性肛门直肠畸形。在本报告中,男性与男性之间的传递支持常染色体显性遗传,这使我们能够排除X连锁的TBX22基因。使用位于LGR5附近的短串联重复标记进行连锁分析排除了该基因作为潜在候选基因。这些结果表明舌系带过短存在遗传异质性。需要对更多家族进行进一步研究以鉴定新的候选基因。