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Xq22.3q23 微缺失,包含 TMEM164 和 AMMECR1 基因:两例病例报告证实存在可识别的表型,表现为身材矮小、中面部发育不良、智力发育迟缓以及椭圆形红细胞增多症。

Xq22.3q23 microdeletion harboring TMEM164 and AMMECR1 genes: Two case reports confirming a recognizable phenotype with short stature, midface hypoplasia, intellectual delay, and elliptocytosis.

机构信息

Département de Génétique et Procréation, Centre Hospitalo-Universitaire Grenoble Alpes, Grenoble Cedex, France.

Univ. Grenoble Alpes, Inserm, U1216, CHU Grenoble Alpes, GIN, 38000 Grenoble, France.

出版信息

Am J Med Genet A. 2019 Apr;179(4):650-654. doi: 10.1002/ajmg.a.61057. Epub 2019 Feb 8.

DOI:10.1002/ajmg.a.61057
PMID:30737907
Abstract

The AMME syndrome defined as the combination of Alport syndrome, intellectual disability, midface hypoplasia, and elliptocytosis (AMME) is known to be a contiguous gene syndrome associated with microdeletions in the region Xq22.3q23. Recently, using exome sequencing, missense pathogenic variants in AMMECR1 have been associated with intellectual disability, midface hypoplasia, and elliptocytosis. In these cases, AMMECR1 gene appears to be responsible for most of the clinical features of the AMME syndrome except for Alport syndrome. In this article, we present two unrelated male patients with short stature, mild intellectual disability or neurodevelopmental delay, sensorineural hearing loss, and elliptocytosis harboring small microdeletions identified by array-CGH involving TMEM164 and AMMECR1 genes and SNORD96B small nucleolar RNA for one patient, inherited from their mothers. These original cases further confirm that most specific AMME features are ascribed to AMMECR1 haploinsufficiency. These cases reporting the smallest microdeletions encompassing AMMECR1 gene provide new evidence for involvement of AMMECR1 in the AMME phenotype and permit to discuss a phenotype related to AMMECR1 haploinsufficiency: developmental delay/intellectual deficiency, midface hypoplasia, midline defect, deafness, and short stature.

摘要

AME 综合征定义为 Alport 综合征、智力障碍、中面部发育不全和椭圆形红细胞增多症(AME)的组合,已知是与 Xq22.3q23 区域微缺失相关的连续基因综合征。最近,使用外显子组测序,在 AMMECR1 中发现错义致病性变异与智力障碍、中面部发育不全和椭圆形红细胞增多症相关。在这些情况下,AMMECR1 基因似乎负责 AME 综合征的大部分临床特征,除了 Alport 综合征。在本文中,我们介绍了两例无关的男性患者,他们具有身材矮小、轻度智力障碍或神经发育迟缓、感觉神经性听力损失和椭圆形红细胞增多症,这些患者携带由其母亲遗传的 TMEM164 和 AMMECR1 基因以及 SNORD96B 小核仁 RNA 的小微缺失,通过微阵列-CGH 鉴定。这些原始病例进一步证实,大多数特定的 AME 特征归因于 AMMECR1 杂合不足。这些报道包含 AMMECR1 基因的最小微缺失的病例为 AMMECR1 参与 AME 表型提供了新的证据,并允许讨论与 AMMECR1 杂合不足相关的表型:发育迟缓/智力缺陷、中面部发育不全、中线缺陷、耳聋和身材矮小。

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