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.

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ژورنال

عنوان ژورنال: Arquivos De Neuro-psiquiatria

سال: 2023

ISSN: ['1678-4227', '0004-282X']

DOI: https://doi.org/10.1055/s-0043-1774589