Molecular genetics of functional articulation disorder in children.
- Author:
Yun-Jing ZHAO
1
;
Hong-Wei MA
Author Information
1. Department of Developmental Pediatrics, Shengjing Hospital of China Medical University, Shenyang, China.
- Publication Type:Journal Article
- MeSH:
Articulation Disorders;
genetics;
Chromosomes, Human, Pair 15;
Chromosomes, Human, Pair 3;
Chromosomes, Human, Pair 6;
Forkhead Transcription Factors;
genetics;
Genetic Predisposition to Disease;
Humans
- From:
Chinese Journal of Contemporary Pediatrics
2012;14(4):316-320
- CountryChina
- Language:Chinese
-
Abstract:
Genetic factors are an important cause of functional articulation disorder in children. This article reviews some genes and chromosome regions associated with a genetic susceptibility to functional articulation disorders. The forkhead box P2 (FOXP2) gene on chromosome 7 is introduced in details including its structure, expression and function. The relationship between the FOXP2 gene and developmental apraxia of speech is discussed. As a transcription factor, FOXP2 gene regulates the expression of many genes. CNTNAP2 as an important target gene of FOXP2 is a key gene influencing language development. Functional articulation disorder may be developed to dyslexia, therefore some candidate regions and genes related to dyslexia, such as 3p12-13, 15q11-21, 6p22 and 1p34-36, are also introduced. ROBO1 gene in 3p12.3, ZNF280D gene, TCF12 gene, EKN1 gene in 15q21, and KIAA0319 gene in 6p22 have been candidate genes for the study of functional articulation disorder.
