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单一上颌中切牙正中畸形:新数据与突变综述

Single median maxillary central incisor: new data and mutation review.

作者信息

El-Jaick Kênia B, Fonseca Renata F, Moreira Miguel A, Ribeiro Márcia G, Bolognese Ana M, Dias Sânia O, Pereira Eliane T, Castilla Eduardo E, Orioli Iêda M

机构信息

Estudo Latino Americano de Malformações Congênitas, Departamento de Genética, Universidade Federal do Rio de Janeiro, Brazil.

出版信息

Birth Defects Res A Clin Mol Teratol. 2007 Aug;79(8):573-80. doi: 10.1002/bdra.20380.

Abstract

BACKGROUND

Single median maxillary central incisor (SMMCI) is a rare anomaly that may occur alone or associated with other conditions, frequently as part of the holoprosencephaly (HPE) spectrum. However, it has been suggested that SMMCI alone, or associated with some midline defects, may be considered a different entity from HPE (OMIM: 147250). Families with SMMCI, without HPE cases, are difficult to counsel for the risk of HPE in future generations because the same midline defects described as part of the "SMMCI syndrome" can also be part of the HPE spectrum.

METHODS

We screened five cases of SMMCI for mutations in three HPE genes, SHH, TGIF, and SIX3.

RESULTS

A missense mutation c.686C>T was found in the gene SIX3 of one patient, which did not differ from the accepted 20% of known HPE gene mutations among all HPE cases. Our results and an extensive literature review of gene mutations in patients with SMMCI showed that 27/28 of them were in HPE genes: SHH (n = 21), SIX3 (n = 3), TGIF (n = 1), GLI2 (n = 1), and PTCH (n = 1), and only one in the SALL4 gene.

CONCLUSIONS

The clinical findings in patients with SMMCI without HPE in families with mutations in HPE genes cannot be distinguished from the findings reported in the SMMCI syndrome. Therefore, persons with SMMCI and their relatives should be carefully investigated for related midline disorders, especially of the HPE spectrum, and all known HPE genes screened.

摘要

背景

单颗上颌中切牙(SMMCI)是一种罕见的异常情况,可能单独出现或与其他病症相关,常作为全前脑畸形(HPE)谱系的一部分。然而,有人提出单独的SMMCI或与某些中线缺陷相关的情况,可能被认为是与HPE(OMIM:147250)不同的实体。没有HPE病例的SMMCI家族很难就后代患HPE的风险提供咨询,因为被描述为“SMMCI综合征”一部分的相同中线缺陷也可能是HPE谱系的一部分。

方法

我们对5例SMMCI患者进行筛查,检测三个HPE基因SHH、TGIF和SIX3中的突变。

结果

在一名患者的SIX3基因中发现了一个错义突变c.686C>T,这与所有HPE病例中已知的HPE基因突变的20%没有差异。我们的结果以及对SMMCI患者基因突变的广泛文献综述表明,其中27/28例患者的突变存在于HPE基因中:SHH(n = 21)、SIX3(n = 3)、TGIF(n = 1)、GLI2(n = 1)和PTCH(n = 1),只有1例存在于SALL4基因中。

结论

在有HPE基因突变的家族中,无HPE的SMMCI患者的临床发现与SMMCI综合征中报道的发现无法区分。因此,应对SMMCI患者及其亲属仔细检查相关的中线疾病,尤其是HPE谱系相关疾病,并对所有已知的HPE基因进行筛查。

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