Publications by authors named "Norah A Alharbi"
Article Synopsis
- Chromosome 16p11.2 deletions and duplications are significant genetic variations linked to a range of clinical outcomes, including developmental delays and autism spectrum disorders, with phenotypic differences among individuals.
- This study identified a de novo recurrent deletion in a Saudi girl, leading to severe cognitive and motor disabilities, alongside rare symptoms like optic atrophy and Dandy-Walker spectrum features.
- The research aims to enhance understanding of genetic disorders in the MENA region, highlighting the unique genetic variations present despite the rarity of these conditions.
Objectives: To determine the prevalence of depression and anxiety in adult multiple sclerosis patients attending tertiary facilities in Riyadh, Saudi Arabia.
Methods: This is a cross-sectional study conducted among MS patients in Riyadh City, Saudi Arabia. A self-administered questionnaire was distributed among MS patients at Prince Sultan Military Medical City in Riyadh, Saudi Arabia between April 2020 and January 2021.