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EDAR 诱导性少汗型外胚层发育不良:杂合 c.1072C>T 突变个体的体征和症状的临床研究。

EDAR-induced hypohidrotic ectodermal dysplasia: a clinical study on signs and symptoms in individuals with a heterozygous c.1072C > T mutation.

机构信息

Pediatric Dentistry, Department of Odontology, Faculty of Medicine, Umeå University, Umeå, Sweden.

出版信息

BMC Med Genet. 2014 May 16;15:57. doi: 10.1186/1471-2350-15-57.

Abstract

BACKGROUND

Mutations in the EDAR-gene cause hypohidrotic ectodermal dysplasia, however, the oral phenotype has been described in a limited number of cases. The aim of the present study was to clinically describe individuals with the c.1072C > T mutation (p. Arg358X) in the EDAR gene with respect to dental signs and saliva secretion, symptoms from other ectodermal structures and to assess orofacial function.

METHODS

Individuals in three families living in Sweden, where some members had a known c.1072C > T mutation in the EDAR gene with an autosomal dominant inheritance (AD), were included in a clinical investigation on oral signs and symptoms and self-reported symptoms from other ectodermal structures (n = 37). Confirmation of the c.1072C > T mutation in the EDAR gene were performed by genomic sequencing. Orofacial function was evaluated with NOT-S.

RESULTS

The mutation was identified in 17 of 37 family members. The mean number of missing teeth due to agenesis was 10.3 ± 4.1, (range 4-17) in the mutation group and 0.1 ± 0.3, (range 0-1) in the non-mutation group (p < 0.01). All individuals with the mutation were missing the maxillary lateral incisors and one or more of the mandibular incisors; and 81.3% were missing all four. Stimulated saliva secretion was 0.9 ± 0.5 ml/min in the mutation group vs 1.7 ± 0.6 ml/min in the non-mutation group (p < 0.01). Reduced ability to sweat was reported by 82% in the mutation group and by 20% in the non-mutation group (p < 0.01). The mean NOT-S score was 3.0 ± 1.9 (range 0-6) in the mutation group and 1.5 ± 1.1 (range 0-5) in the non-mutation group (p < 0.01). Lisping was present in 56% of individuals in the mutation group.

CONCLUSIONS

Individuals with a c.1072C > T mutation in the EDAR-gene displayed a typical pattern of congenitally missing teeth in the frontal area with functional consequences. They therefore have a need for special attention in dental care, both with reference to tooth agenesis and low salivary secretion with an increased risk for caries. Sweating problems were the most frequently reported symptom from other ectodermal structures.

摘要

背景

EDAR 基因突变会导致少汗型外胚层发育不良,但口腔表型在少数病例中有描述。本研究的目的是临床描述携带 EDAR 基因 c.1072C>T 突变(p.Arg358X)的个体的牙齿特征和唾液分泌情况、其他外胚层结构的症状,并评估口颌功能。

方法

在瑞典的三个家族中,有一些成员携带已知的 EDAR 基因 c.1072C>T 突变,表现为常染色体显性遗传(AD),这些家族的成员参与了口腔症状和体征以及其他外胚层结构的自报告症状的临床研究(n=37)。通过基因组测序证实 EDAR 基因中的 c.1072C>T 突变。NOT-S 用于评估口颌功能。

结果

37 名家族成员中发现 17 名携带该突变。突变组因缺失导致的缺牙平均数为 10.3±4.1(范围 4-17),而非突变组为 0.1±0.3(范围 0-1)(p<0.01)。所有携带该突变的个体均缺失上颌侧切牙和/或下颌切牙;81.3%的个体缺失全部四颗。突变组的刺激唾液分泌量为 0.9±0.5 ml/min,而非突变组为 1.7±0.6 ml/min(p<0.01)。82%的突变组报告有出汗减少的情况,而非突变组为 20%(p<0.01)。突变组的 NOT-S 评分均值为 3.0±1.9(范围 0-6),而非突变组为 1.5±1.1(范围 0-5)(p<0.01)。突变组中有 56%的个体存在口齿不清。

结论

携带 EDAR 基因 c.1072C>T 突变的个体在前额区域表现出典型的先天性缺牙模式,具有功能后果。因此,他们在口腔保健方面需要特别关注,既要注意牙齿缺失,又要注意唾液分泌减少导致的龋齿风险增加。其他外胚层结构的症状中,出汗问题是最常报告的症状。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9e43/4036832/86aa723c599a/1471-2350-15-57-1.jpg

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