Neurodevelopmental disorder associated with the DOCK7 gene
نویسندگان
چکیده
Case presentation: PHAPS, male, 9 years old, being followed up at the neuropediatric outpatient clinic for a history of seizures since 1 year and 6 months, focal epilepsy with in type left side, eyelid myoclonus drooling, subsequent generalization. At seven he started behavioral changes stereotypies. Delayed neuropsychomotor development: sustained cervical 3 lallation year, articulation first words language sentence formation only 7 years. Past pathological history: born term, normal delivery without complications. Physical examination: patient little contact, low implantation ears high-arched palate. Neurological examination deficit, preserved reflexes, atypical gait, muscle strength grade 5, tone, cranial nerves alterations. Complementary exams: Cranial magnetic resonance imaging: right mesial temporal sclerosis. Video-electroencephalogram: epileptiform paroxysms diffuse projection hemispheric accentuation on right, posterior regions occurring synchronously asynchronously, predominantly left. CGH-ARRAY genomic comparison analysis: normal. Exome sequencing: heterozigosy mutation DOCK gene (chr1:62.954.634 G>GA chr1:63.091.022 G>A). Clinical significancy: likely pathogenic mutation.
منابع مشابه
Epilepsy as a Neurodevelopmental Disorder
Epilepsy is characterized by spontaneous recurrent seizures and comprises a diverse group of syndromes with different etiologies. Epileptogenesis refers to the process whereby the brain becomes epileptic and can be related to several factors, such as acquired structural brain lesions, inborn brain malformations, alterations in neuronal signaling, and defects in maturation and plasticity of neur...
متن کاملBiological mechanisms associated with increased perseveration and hyperactivity in a genetic mouse model of neurodevelopmental disorder
Chromosomal deletions at Xp22.3 appear to influence vulnerability to the neurodevelopmental disorders attention deficit hyperactivity disorder (ADHD) and autism. 39,X(Y*)O mice, which lack the murine orthologue of the Xp22.3 ADHD candidate gene STS (encoding steroid sulfatase), exhibit behavioural phenotypes relevant to such disorders (e.g. hyperactivity), elevated hippocampal serotonin (5-HT) ...
متن کاملAltered synaptobrevin-II trafficking in neurons expressing a synaptophysin mutation associated with a severe neurodevelopmental disorder
Following exocytosis, synaptic vesicles (SVs) have to be reformed with the correct complement of proteins in the correct stoichiometry to ensure continued neurotransmission. Synaptophysin is a highly abundant, integral SV protein necessary for the efficient retrieval of the SV SNARE protein, synaptobrevin II (sybII). However the molecular mechanism underpinning synaptophysin-dependent sybII ret...
متن کاملCHD8 regulates neurodevelopmental pathways associated with autism spectrum disorder in neural progenitors.
Truncating mutations of chromodomain helicase DNA-binding protein 8 (CHD8), and of many other genes with diverse functions, are strong-effect risk factors for autism spectrum disorder (ASD), suggesting multiple mechanisms of pathogenesis. We explored the transcriptional networks that CHD8 regulates in neural progenitor cells (NPCs) by reducing its expression and then integrating transcriptome s...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: Arquivos De Neuro-psiquiatria
سال: 2023
ISSN: ['1678-4227', '0004-282X']
DOI: https://doi.org/10.1055/s-0043-1774589