ALAA ALAYED
Riyadh,Saudi Arabia
Summary
Dedicated pediatrician with five years of experience in clinical genetics and metabolic diseases. Expertise in delivering precise and attentive care, ensuring patient concerns are addressed clearly and effectively. Collaborative team player committed to enhancing patient satisfaction through open communication and input from colleagues. Fellowship training as a clinical geneticist provides strong clinical and scientific foundation for independent practice.
Overview
13
13
years of professional experience
Work history
Consultant
Riyadh hospital
Riyadh
2026.01 - Current
Consultatnt
Alhabib medical group
Riyadh
2025.02 - 2025.05
Consultant
Maternity and Children Hospital
Buridah
2022.02 - 2023.05
- Provided support for over 200 patients with metabolic diseases.
- Assisted approximately 20 patients undergoing enzyme replacement therapy for lysosomal storage diseases.
- Conducted over 4000 newborn screening tests.
- Facilitated follow-up care for more than 4000 patients in genetic clinics.
Fellow
King Fahad Medical City
Riyadh
2019.01 - 2021.12
- Successfully diagnosed and treated a wide spectrum of genetic diseases, leading to improved patient outcomes.
Enhanced enzyme replacement therapy protocols, increasing treatment efficacy for specific genetic disorders.
Developed and executed a comprehensive genetic counselling and prevention programme, benefitting numerous families.
Interpreted over 2000 genetic tests, providing effective management recommendations and enhancing patient care.
Resident
Maternity and Children Hospital
Buridah
2012.10 - 2016.10
Education
Saudi Fellowship - Clinical Genetics and Metabolic disorders
King Fahad Medical City
Saudi ArabiaSaudi Board - Pediatrics
Qassim Maternity and Children hospital
Saudi ArabiaBachelor degree - Medicine and Surgery
College of medicine at Qassim university
Saudi ArabiaSkills
- Genetic diagnosis and treatment
- Genetic testing interpretation
- Genetic counseling
- Enzyme replacement therapy
Publications
- Case Report: Metabolic acidosis and Hypoglycemia in a Child with Leigh-like Phenotype, Clinical Chemistry Journal, 2019
- Case Report: Harel-Yoon syndrome: The first Case Report from Saudi Arabia, Journal of Saudi Biochemical and Clinical Genetics, 2020
- Clinical and Genetic Phenotypes of Hepatic Glycogen Storage Disease: a Multicenter experience, King Fahad Medical City, 2021
- Case Report: Successful Treatment with uridine in CAD related disorders, International Conference of European society of Human genetics, 2021
References
- Dr. Mohammed Al-manaie, King Abdullah Specialized Children's Hospital, (+9661) 801-1111 ext. 53215, almannaimo@ngha.med.sa
- Dr. Mohammed Saleh, King Fahad Medical City, (+966) 112889999 Ext: 25351, Msaleh@kfmc.med.sa
- Dr. Aziza M. Mushiba, King Fahad Medical City, (+966) 112889999 Ext: 25122, Amushiba@kfmc.med.sa
Timeline
Consultant
Riyadh hospital
2026.01 - Current
Consultatnt
Alhabib medical group
2025.02 - 2025.05
Consultant
Maternity and Children Hospital
2022.02 - 2023.05
Fellow
King Fahad Medical City
2019.01 - 2021.12
Resident
Maternity and Children Hospital
2012.10 - 2016.10
Saudi Board - Pediatrics
Qassim Maternity and Children hospital
Saudi Fellowship - Clinical Genetics and Metabolic disorders
King Fahad Medical City
Bachelor degree - Medicine and Surgery
College of medicine at Qassim university