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Identification of a novel METTL23 gene variant in a patient with an intellectual development disorder: a literature review and case report.
Zha, Jian; Chen, Yong; Cao, Fangfang; Yu, Yanghong; Wang, Ruiyan; Zhong, Jianmin.
Afiliación
  • Zha J; Department of Neurology, Jiangxi Provincial Children's Hospital, Nanchang, China.
  • Chen Y; Department of Neurology, Jiangxi Provincial Children's Hospital, Nanchang, China.
  • Cao F; Department of Neurology, Jiangxi Provincial Children's Hospital, Nanchang, China.
  • Yu Y; Department of Radiology, Jiangxi Provincial Children's Hospital, Nanchang, China.
  • Wang R; Department of Neurology, Jiangxi Provincial Children's Hospital, Nanchang, China.
  • Zhong J; Department of Neurology, Jiangxi Provincial Children's Hospital, Nanchang, China.
Front Pediatr ; 12: 1328063, 2024.
Article en En | MEDLINE | ID: mdl-39026940
ABSTRACT
METTL23 belongs to a family of protein lysine methyltransferases that methylate non-histone proteins. Recently, the METTL23 gene has been reported to be related to an intellectual developmental disorder, autosomal recessive 44. Patients present with developmental delay, intellectual disability (ID), and variable dysmorphic features. Here, we report on a Chinese girl who presented with global developmental delay, abnormal brain structure, and multiple facial deformities, including a short/upturned nose with a sunken bridge, thin lips, and flat occiput. Whole-exome sequencing identified a novel variant (NM_001080510.5 c.322+1del) on the METTL23 gene. This variant was not collected on public human variants databases such as gnomAD, predicted to influence the splicing as a classical splicing variant, and classified as Pathogenic according to the American College of Medical Genetics and Genomics (ACMG) guidelines. Since patients with METTL23-related ID are rare, we summarize and compare the clinical phenotype of reported patients with METTL23 variants. Our report further expands the METTL23 variants and provides new evidence for clinical diagnosis of METTL23-related ID.
Palabras clave

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Front Pediatr Año: 2024 Tipo del documento: Article País de afiliación: China Pais de publicación: Suiza

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Front Pediatr Año: 2024 Tipo del documento: Article País de afiliación: China Pais de publicación: Suiza