Publications by authors named "Faten Abdullah AlRadini"
Correction: Chromosome 16p11.2 microdeletion syndrome with microcephaly and Dandy-Walker malformation spectrum: expanding the known phenotype.
Liena Elbaghir Omer Elsayed Norah Ayed AlHarbi Ashwaq Mohammed Alqarni Huda Hussein Elwasila Eltayeb Noura Mostafa Mohamed Mostafa Faten Abdullah AlRadini
Hum Genomics
October 2024
Chromosome 16p11.2 microdeletion syndrome with microcephaly and Dandy-Walker malformation spectrum: expanding the known phenotype.
Liena Elbaghir Omer Elsayed Norah Ayed AlHarbi Ashwaq Mohammed Alqarni Huda Hussein Elwasila Eltayeb Noura Mostafa Mohamed Mostafa Faten Abdullah AlRadini
Hum Genomics
September 2024
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.
Background: Medical simulation is an effective educational tool used to increase confidence, improve knowledge, and refine skills when responding to high-acuity situations. Despite established roles of the pharmacist on the hospital code team, most institutions lack formalized pharmacist training for code team responses.
Objective: This pre-post analysis aimed to evaluate the impact of a didactic and simulation-based code response training for pharmacists on self-perceived improvement and preparedness when responding to in-hospital medical emergencies.