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Four novel mutations of FAM20A in amelogenesis imperfecta type IG and review of literature for its genotype and phenotype spectra

机译:Amelogenesis Im20A的FAM20A的四种新突变Ig和其基因型和表型光谱的文献综述

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Amelogenesis imperfecta type IG (AI1G) is caused by mutations in FAM20A. Genotypic and phenotypic features of AI1G are diverse and their full spectra remain to be characterized. The aim of this study was to identify and summarize variants in FAM20A in a broad population of patients with AI1G. We identified a Thai female (Pt-1) and a Saudi male (Pt-2) affected with AI1G. Both had hypoplastic enamel, gingival hyperplasia, and intrapulpal calcification. Pt-1 also had rapidly progressive embedding of unerupted teeth, early eruption of permanent teeth, and spontaneous dental infection. Uniquely, Pt-2 had all permanent teeth erupted which was uncommon in AI1G patients. Whole exome sequencing (WES) identified that Pt-1 was heterozygous for FAM20A, c.758A > G (p.Tyr253Cys), inherited from her father. The mutation on maternal allele was not detected by WES. Pt-2 possessed compound heterozygous mutations, c.1248dupG (p.Phe417Valfs*7); c.1081C > T (p.Arg361Cys) in FAM20A. Array comparative genomic hybridization (aCGH), cDNA sequencing, and whole genome sequencing successfully identified 7531 bp deletion on Pt-1's maternal allele. This was the largest FAM20A deletion ever found. A review of all 70 patients from 50 independent families with AI1G (including two families in this study) showed that the penetrance of hypoplastic enamel and gingival hyperplasia was complete. Unerupted permanent teeth were found in all 70 patients except Pt-2. Exons 1 and 11 were mutation-prone. Most mutations were frameshift. Certain variants showed founder effect. To conclude, this study reviews and expands phenotypic and genotypic spectra of AI1G. A large deletion missed by WES can be detected by WGS. Hypoplastic enamel, gingival hyperplasia, and unerupted permanent teeth prompt genetic testing of FAM20A. Screening of nephrocalcinosis, early removal of embedded teeth, and monitoring of dental infection are recommended.
机译:Amelogesesis Imperfecta型Ig(AI1G)是由FAM20A中的突变引起的。 AI1G的基因型和表型特征是不同的,其全谱仍然是特征。本研究的目的是识别和总结FAM20A中的VARIANTS,在广泛的AI1G患者中。我们确定了泰国女性(PT-1)和AI1G影响的沙特雄性(PT-2)。两者都有皮下釉质,牙龈增生和血管钙化。 PT-1还迅速逐渐嵌入未牙齿,恒牙早期喷发,以及自发的牙科感染。唯一的是,PT-2爆发的所有常牙牙齿都爆发,在AI1G患者中罕见。全外壳测序(WES)鉴定为FAM20A,C.758A> G(P.TYR253CYS)的杂合子,从她父亲继承。 WES未检测到母体等位基因的突变。 PT-2具有化合物杂合突变,C.1248Dupg(P.phe417Valfs * 7); C.1081C> FAM20A中的T(P.ARG361CYS)。阵列对比基因组杂交(ACGH),cDNA测序和全基因组测序成功鉴定了PT-1母体等位基因的7531bp缺失。这是有史以来最大的FAM20A删除。对所有70名与AI1G的独立家庭患者(包括这项研究中的两个家庭)的审查表明,Hypoplastic珐琅和牙龈增生的渗透完成。除了PT-2外,在所有70例患者中发现了未造成的永久性牙齿。外显子1和11是突变的。大多数突变是越来越的。某些变体显示出创始人效果。为了得出结论,这项研究和扩展了AI1G的表型和基因型光谱。 WES错过的大型删除可以通过WGS来检测。发育不全的牙釉质,牙龈增生,和未延伸的永久性牙齿迅速遗传测试FAM20A。建议筛选肾癌,早期去除嵌入牙齿,以及牙科感染监测。

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