Autism Spectrum Disorder (ASD) and Attention Deficit Hyperactivity Disorder (ADHD) With Language Impairment Accompanied by Developmental Disability Caused by Forkhead Box Protein 1 (FOXP1) Exon Deletion: A Case Report-Reference-Cited by-同舟云学术

Autism Spectrum Disorder (ASD) and Attention Deficit Hyperactivity Disorder (ADHD) With Language Impairment Accompanied by Developmental Disability Caused by Forkhead Box Protein 1 (FOXP1) Exon Deletion: A Case Report

Published:2021-12-22 Issue: Volume: Page:
ISSN:2168-8184
Container-title:Cureus
language:en
Short-container-title:

Author:

Alenezi Shuliweeh,Alyahya Ahmed,Aldhalaan Hesham

Publisher

Cureus, Inc.

Subject

Aerospace Engineering

Reference7 articles.

1. FOXP1 syndrome: a review of the literature and practice parameters for medical assessment and monitoring;Lozano R.;J Neurodev Disord 13,2021

2. Autism with dysphasia accompanied by mental retardation caused by FOXP1 exon deletion: a case report;Lin SZ;World J Clin Cases,2021

3. Individuals with FOXP1 syndrome present with a complex neurobehavioral profile with high rates of ADHD, anxiety, repetitive behaviors, and sensory symptoms;Trelles MP;Mole Aut,2021

4. Novel FOXP1 pathogenic variants in two Indian subjects with syndromic intellectual disability;Moirangthem A;Am J Med Genet A,2021

5. Peruvian newborn male with 3p13 deletion syndrome encompassing the FOXP1 gene: review of the literature;Abarca-Barriga HH;J Pediatr Genet,2020

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1. Clinical Characteristics and Whole Exome Sequencing Analysis in Serbian Cases of Clubfoot Deformity—Single Center Study;Children;2024-05-27

2. Compensation between FOXP transcription factors maintains proper striatal function;Cell Reports;2024-05

3. Clinical phenotype of FOXP1 syndrome: parent-reported medical signs and symptoms in 40 individuals;Journal of Medical Genetics;2023-12-16

4. Cortex-restricted deletion of Foxp1 impairs barrel formation and induces aberrant tactile responses in a mouse model of autism;Molecular Autism;2023-09-11

5. A Review on the Role of Genetic Mutations in the Autism Spectrum Disorder;Molecular Neurobiology;2023-06-06