天冬氨酸糖氨基尿患者的特征性牙弓和牙咬合。

P Arvio, M Arvio, S Pirinen
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摘要

天门冬氨酸糖氨基尿症(AGU)是一种溶酶体积存障碍,以进行性智力迟钝为主要表现。这种疾病是由编码天冬氨酸氨基葡萄糖酶(AGA)基因的单核苷酸变化引起的。这种罕见的疾病在芬兰相对常见:我们能够检查81名芬兰aguu患者的牙齿和口腔变化。牙冠大小和牙冠形状正常,但牙合错误很常见,牙间距、大覆盖、前开牙合和侧交叉牙合的患病率超过芬兰人群的患病率(P < 0.0001)。儿童时期的牙弓已经很大,而在成年患者中,与芬兰人口标准相比,下牙弓在所有维度上都更大(P < 0.001)。几乎所有的患者都有异常大的舌头,我们认为这是结构异常的原因。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Characteristic dental arches and occlusion in patients with aspartylglucosaminuria.

Aspartylglucosaminuria (AGU) is a lysosomal storage disorder with progressive mental retardation as a presenting manifestation. The disorder is caused by a single nucleotide change in the gene encoding aspartylglucosaminidase (AGA). This rare disease is relatively common in Finland: we were able to examine 81 Finnish AGU-patients for dental and oral changes. Tooth crown size and crown shape were normal, but dental malocclusions were common, and prevalences of spacing, large overjet, anterior open bite, and lateral crossbite exceeded Finnish population prevalences (P < 0.0001). Dental arches were already large in childhood, and in adult patients, when compared to Finnish population standards, the lower dental arch was larger in all dimensions (P < 0.001). Almost all patients had abnormally large tongues, which we assumed to be the reason for the structural abnormalities observed.

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