Development Delay | List of Frontiers open access articles

Original Research

Published on 22 Nov 2024

Association between reported ADHD symptom and motor development delay in preschool children

in Children and Health

Zhijun Cui
Shijie Li
Aimin Liang
Hongmei Huang
Xin Ni

Frontiers in Pediatrics

doi 10.3389/fped.2024.1480488

4,935 views
2 citations

Original Research

Published on 09 Jan 2023

Potential dynamic regional brain biomarkers for early discrimination of autism and language development delay in toddlers

in Brain Imaging Methods

Shengjuan Wu
Zhi Wen
Wenzhong Yang
Chengcheng Jiang
Yurong Zhou
Zhiwei Zhao
Aiqin Zhou
Xinglian Liu
Xiaoyan Wang
Yue Wang

Frontiers in Neuroscience

doi 10.3389/fnins.2022.1097244

4,068 views
9 citations

Original Research

Published on 03 Nov 2021

New Approach to Intelligence Screening for Children With Global Development Delay Using Eye-Tracking Technology: A Pilot Study

in Pediatric Neurology

Hong Xu
Xiaoyan Xuan
Li Zhang
Wenxin Zhang
Min Zhu
Xiaoke Zhao

Frontiers in Neurology

doi 10.3389/fneur.2021.723526

7,958 views
8 citations

Original Research

Published on 21 Mar 2023

A novel SETD2 variant causing global development delay without overgrowth in a Chinese 3-year-old boy

in Genetics of Common and Rare Diseases

Yuanyuan Wu
Fang Liu
Ruihua Wan
Baoquan Jiao

Frontiers in Genetics

doi 10.3389/fgene.2023.1153284

9,621 views
9 citations

Case Report

Published on 11 Jul 2022

Case Report: Identification of Two Variants of ALG13 in Families With or Without Seizure and Binocular Strabismus: Phenotypic Spectrum Analysis

in Genetics of Common and Rare Diseases

Tao Cai
Jieting Huang
Xiuwei Ma
Siqi Hu
Lina Zhu
Jinwen Zhu
Zhichun Feng

Frontiers in Genetics

doi 10.3389/fgene.2022.892940

4,096 views
7 citations

Original Research

Published on 21 Apr 2021

Mutations in RNA Methyltransferase Gene NSUN5 Confer High Risk of Outflow Tract Malformation

in Molecular and Cellular Pathology

Yifeng Wang
Tao Jiang
Jiani Xu
Yayun Gu
Yan Zhou
Yuan Lin
Yifei Wu
Wei Li
Cheng Wang
Bin Shen

Frontiers in Cell and Developmental Biology

doi 10.3389/fcell.2021.623394

6,580 views
17 citations

Case Report

Published on 08 May 2018

Homozygous PIGT Mutation Lead to Multiple Congenital Anomalies-Hypotonia Seizures Syndrome 3

in Genetics of Common and Rare Diseases

Li Yang
Jing Peng
Xiao-Meng Yin
Nan Pang
Chen Chen
Teng-Hui Wu
Xiao-Min Zou
Fei Yin

Frontiers in Genetics

doi 10.3389/fgene.2018.00153

9,517 views
26 citations

Case Report

Published on 14 Apr 2021

Case Report: Expanding Clinical, Immunological and Genetic Findings in Sideroblastic Anemia With Immunodeficiency, Fevers and Development Delay (SIFD) Syndrome

in Autoimmune and Autoinflammatory Disorders

Leonardo Oliveira Mendonca
Alex Isidoro Prado
Izelda Maria Carvalho Costa
Marcia Bandeira
Rafael Dyer
Samar Freschi Barros
Karen Francine Khöler
Luiz Augusto Marcondes Fonseca
Jorge Kalil
Fabio Morato Castro

Frontiers in Immunology

doi 10.3389/fimmu.2021.586320

4,883 views
9 citations

Original Research

Published on 28 Aug 2025

Analysis of the impact of parents' electronic screen time habits, young children's screen exposure and parent-child interaction on language development delay in young children

in Children and Health

Xiaohong Wan
Xiaoqing Kang
Shunli Chen
Juan Du
Fang Yan
Yongqi Bai

Frontiers in Pediatrics

doi 10.3389/fped.2025.1667048

8,144 views
2 citations

Original Research

Published on 16 Nov 2023

Association between parents’ concerns about eating and sleeping problems and social-emotional development in Chinese children aged 3 to 6 years

in Children and Health

Tongxi Hu
Shaoying Liu
Jianying Zhan
Luxin Xu
Yanqing Zhou

Frontiers in Public Health

doi 10.3389/fpubh.2023.1264219

3,006 views
1 citation

Original Research

Published on 24 Dec 2021

De novo STXBP1 Mutations in Two Patients With Developmental Delay With or Without Epileptic Seizures

in Pediatric Neurology

Ping Yang
Robert Broadbent
Chitra Prasad
Simon Levin
Sharan Goobie
Joan H. Knoll
Asuri N. Prasad

Frontiers in Neurology

doi 10.3389/fneur.2021.804078

5,539 views
3 citations

Original Research

Published on 11 Apr 2019

Neurological Diseases With Autism Spectrum Disorder: Role of ASD Risk Genes

in Neurogenomics

Juan Xiong
Shimeng Chen
Nan Pang
Xiaolu Deng
Lifen Yang
Fang He
Liwen Wu
Chen Chen
Fei Yin
Jing Peng

Frontiers in Neuroscience

doi 10.3389/fnins.2019.00349

33,145 views
62 citations

Original Research

Published on 30 Sep 2021

A Chinese Case of Cornelia de Lange Syndrome Caused by a Pathogenic Variant in SMC3 and a Literature Review

in Pediatric Endocrinology

Ran Li
Bowen Tian
Hanting Liang
Meiping Chen
Hongbo Yang
Linjie Wang
Hui Pan
Huijuan Zhu

Frontiers in Endocrinology

doi 10.3389/fendo.2021.604500

5,582 views
9 citations

Original Research

Published on 29 Jul 2024

A novel autism-associated KCNB1 mutation dramatically slows Kv2.1 potassium channel activation, deactivation and inactivation

in Cellular Neuropathology

Rían W. Manville
Samantha D. Block
Claire L. Illeck
Jessica Kottmeier
Richard Sidlow
Geoffrey W. Abbott

Frontiers in Cellular Neuroscience

doi 10.3389/fncel.2024.1438101

5,058 views
6 citations

Original Research

Published on 13 Dec 2022

Phenotype and genotype analyses of Chinese patients with autosomal dominant mental retardation type 5 caused by SYNGAP1 gene mutations

in Genetics of Common and Rare Diseases

Yanxin Wang
Yuqiang Lv
Zilong Li
Min Gao
Xiaomeng Yang
Yue Li
Jianguo Shi
Zaifen Gao
Yi Liu
Zhongtao Gai

Frontiers in Genetics

doi 10.3389/fgene.2022.957915

4,838 views
11 citations

Original Research

Published on 03 Jul 2025

Single-center prospective study on thyroid function outcomes and neurological prognoses at 3 years of age in children with mild neonatal hyperthyrotropinemia

in Pediatric Endocrinology

Guoyu Sun
Rui Zhang
Jianing Zhang
Yanxia Zhou
Zezhong Tang
Lili Liu
Xinlin Hou

Frontiers in Endocrinology

doi 10.3389/fendo.2025.1548086

2,606 views

Articles

Association between reported ADHD symptom and motor development delay in preschool children

Potential dynamic regional brain biomarkers for early discrimination of autism and language development delay in toddlers

New Approach to Intelligence Screening for Children With Global Development Delay Using Eye-Tracking Technology: A Pilot Study

A novel SETD2 variant causing global development delay without overgrowth in a Chinese 3-year-old boy

Case Report: Identification of Two Variants of ALG13 in Families With or Without Seizure and Binocular Strabismus: Phenotypic Spectrum Analysis

Mutations in RNA Methyltransferase Gene NSUN5 Confer High Risk of Outflow Tract Malformation

Homozygous PIGT Mutation Lead to Multiple Congenital Anomalies-Hypotonia Seizures Syndrome 3

Case Report: Expanding Clinical, Immunological and Genetic Findings in Sideroblastic Anemia With Immunodeficiency, Fevers and Development Delay (SIFD) Syndrome

Analysis of the impact of parents' electronic screen time habits, young children's screen exposure and parent-child interaction on language development delay in young children

Association between parents’ concerns about eating and sleeping problems and social-emotional development in Chinese children aged 3 to 6 years

De novo STXBP1 Mutations in Two Patients With Developmental Delay With or Without Epileptic Seizures

Neurological Diseases With Autism Spectrum Disorder: Role of ASD Risk Genes

A Chinese Case of Cornelia de Lange Syndrome Caused by a Pathogenic Variant in SMC3 and a Literature Review

A novel autism-associated KCNB1 mutation dramatically slows Kv2.1 potassium channel activation, deactivation and inactivation

Phenotype and genotype analyses of Chinese patients with autosomal dominant mental retardation type 5 caused by SYNGAP1 gene mutations

Single-center prospective study on thyroid function outcomes and neurological prognoses at 3 years of age in children with mild neonatal hyperthyrotropinemia