Search Results - "Developmental delay"

A Novel MYO5A Mutation (c.3508C>T) in a 27‐Month‐Old Girl With Hypotonia and Developmental Delay: Expanding the Phenotypic Spectrum of Griscelli Syndrome Type 1.

Authors: AmirKashani, Davoud Hosseini, Soudabeh Mojbafan, Marziyeh et al.

Source: Case Reports in Immunology. 6/28/2026, Vol. 2026, p1-4. 4p.

Functional Characterization of Loss of RNF43 Reveals Neuronal Defects in a Caenorhabditis elegans Model.

Authors: Sonmez, Kaan Güzel, Sinem Kazan, Hasan Huseyin et al.

Source: International Journal of Molecular Sciences. May2026, Vol. 27 Issue 10, p4509. 8p.

Genetic and Clinical Characterization of TANGO2 Deficiency Disorder: Insights from the Italian Multicentre Cohort.

Authors: Turco, Emanuela Claudia Pisanò, Giulia Caiazza, Laura et al.

Source: International Journal of Molecular Sciences. May2026, Vol. 27 Issue 10, p4389. 15p.

Imitation in Hispanic/Latine Children with Developmental Delay and Their Caregivers Following a Remote Parenting Intervention.

Authors: Gillenson, Caroline J. Hayes, Timothy Cafatti Mac-Niven, Anastassia et al.

Source: Journal of Clinical Child & Adolescent Psychology. May/Jun2026, Vol. 55 Issue 3, p528-541. 14p.

Subjects: Developmental delay, Acculturation, Hispanic American children, Replication (Experimental design), Socialization, Parenting, Caregiver-child relationships

Association Between Exposure to General Anesthesia and Cognitive and Behavioral Changes in Children Under 6 Years of Age, Undergoing Urogenital Surgery: Prospective Study.

Alternate Title: Ürogenital Cerrahi Geçiren 6 Yaş Altı Çocuklarda Genel Anestezi Maruziyeti ile Bilişsel ve Davranışsal Değişiklikler Arasındaki İlişki: Prospektif Çalışma.

Authors: AYYILDIZ, Didem ÇUFALI, Yelda UYSAL OKAY, Serap et al.

Source: Turkiye Klinikleri Journal of Pediatrics / Türkiye Klinikleri Pediatri Dergisi. 2026, Vol. 35 Issue 2, p69-76. 8p.

Maternal Zika virus exposure and neurodevelopmental outcomes: A longitudinal study of preschool children in the ZIKAlliance Colombian Cohort.

Authors: Herrera, Víctor Miranda, María Consuelo Lozano-Parra, Anyela et al.

Source: PLoS ONE. 4/13/2026, Vol. 21 Issue 4, p1-13. 13p.

Evaluation of the Relationship Between Neonatal Jaundice and Neurodevelopmental Delay in Full-Term Infants.

Authors: Koonuru, Mahesh Kumar Bala, Gopal Venugopal, Satya Prasad et al.

Source: Malaysian Journal of Medicine & Health Sciences. 2026 Supplement, Vol. 22, p94-97. 4p.

Novel Variants in KMT2C Further Support a Neurodevelopmental Disorder Distinct From Kleefstra and Kabuki Syndromes.

Authors: Sedláčková, Lucie Brožková, Dana Šafka Havlovicová, Markéta et al.

Source: Molecular Genetics & Genomic Medicine. Apr2026, Vol. 14 Issue 4, p1-6. 6p.

EEG abnormalities in children with global developmental delay: A retrospective study.

Authors: Albaradie, Raidah Alshammari, Alaa K. Alsubaie, Fatima A. et al.

Source: Journal of Family Medicine & Primary Care. Apr2026, Vol. 15 Issue 4, p1546-1550. 5p.

Neurodevelopmental Profile of a 4.5-Year-Old Girl with Tetrasomy X.

Authors: Marisavljević, Maša Stanojević, Nina Bogavac, Ivana et al.

Source: Pediatric Reports. Apr2026, Vol. 17 Issue 2, p40. 14p.

A Pediatric Case of Neurodevelopmental Delay with a Familial H4C11 Variant: Clinical Course and Diagnostic Challenges.

Authors: Tudorache, Elena Giurgiuveanu, Andreea Severin, Emilia et al.

Source: Journal of Clinical Medicine. Apr2026, Vol. 15 Issue 7, p2505. 9p.

Neurodevelopmental Trajectories at 3 Years: Insights From the NASCITA Italian Birth Cohort.

Authors: Segre, Giulia Roberti, Elisa Campi, Rita et al.

Source: International Journal of Pediatrics. 3/9/2026, Vol. 2026, p1-11. 11p.

Association between obesity and neurodevelopmental delay risk in children under five years: A study from Tumbes, Peru.

Authors: Arredondo-Nontol, Miriam Arredondo-Nontol, Rodolfo Reto, Narcisa et al.

Source: PLoS ONE. 3/6/2026, Vol. 21 Issue 3, p1-20. 20p.

Identification of a Homozygous PGM2L1 Variant in a Male Patient With Developmental Delay and Seizures.

Authors: Niu, Mengmeng Wang, Dong Jia, Shanshan

Source: Molecular Genetics & Genomic Medicine. Mar2026, Vol. 14 Issue 3, p1-5. 5p.

Stress, social participation, and coping strategies in caregivers of children with developmental delay – An observational study.

Authors: Nishanth, J Franklyn, Nirupama N. George, Carolin E.

Source: Journal of Family Medicine & Primary Care. Mar2026, Vol. 15 Issue 3, p1388-1393. 6p.

Pandemic Babies: Developmental Outcomes in Preschool-Aged Children Born During the COVID-19 Era.

Authors: Sade, Sally Gonzalez, Claudia L. R. Gibb, Robbin L.

Source: Behavioral Sciences (2076-328X). Feb2026, Vol. 16 Issue 2, p309. 22p.

Refractory cyclic vomiting syndrome in TUBB3 R262H syndrome: a case report.

Authors: Makkiyah, Rosul Amin, Saista Gupta, Bhavna

Source: Egyptian Pediatric Association Gazette. 1/27/2026, Vol. 74 Issue 1, p1-7. 7p.

Multiple Mitochondrial Dysfunction Syndrome Caused by IBA57 Gene Mutation: A Case Report and Literature Review.

Authors: Xu, Jia Zhang, Xin Hua, Ying et al.

Source: Molecular Genetics & Genomic Medicine. Jan2026, Vol. 14 Issue 1, p1-17. 17p.

Whole Exome Sequencing in Patients With Developmental Delay/Intellectual Disability (DD/ID), Epilepsy and the First Turkish Patient Diagnosed With BCL11A‐Related Intellectual Disability.

Authors: Akkus, Nejmiye Canbal, Abdullah Guneysu, Seda et al.

Source: Molecular Genetics & Genomic Medicine. Jan2026, Vol. 14 Issue 1, p1-16. 16p.

Relation between umbilical cord blood lead level and subsequent neurobehavioral development during infancy.

Authors: Al-Gendy, Fady M. El-Shafie, Ali M. Midan, Dina A. et al.

Source: Alexandria Journal of Pediatrics. Jan-Apr2026, Vol. 39 Issue 1, p1-8. 8p.