Ghayda Mirzaa, MD

Ghayda Mirzaa, MD

Specialties

"When I was growing up in the Middle East, I saw many children who were affected by disorders affecting early brain development, but didn't always have access to good quality medical care. These disorders were often devastating for them and their families, and I resolved to find a way to help. Now, as a physician and a researcher, my goal is to uncover the genes that cause these disorders, understand these conditions better, and to hopefully find better ways to treat and potentially cure them."

  • Biography

    Ghayda Mirzaa, MD, is a pediatrician and researcher who has dedicated her career to helping children and families with developmental brain disorders. As a pediatrician, she delivers the best available treatments, and helps children and families lead the healthiest possible lives. As a researcher, she investigates how genes contribute to neurodevelopmental disorders.

    Mirzaa is an assistant processor of pediatrics and genetics at Seattle Childrens Hospital and the University of Washington, and a principal investigator at the Seattle Childrens Research Institute. She is board-certified in pediatrics, medical genetics and molecular genetics. She received her MD from the Arabian Gulf University (Kingdom of Bahrain), did her residency in pediatrics at the University of Illinois at Chicago, and completed fellowships in human genetics and molecular genetics at the University of Chicago and the University of Washington.

    Board Certification(s)

    Pediatrics
    Medical Genetics, Clinical Molecular Genetics

    Education

    Arabian Gulf University, Manama

    Residency

    University of Illinois at Chicago, Chicago, IL

    Fellowship

    University of Washington, Seattle, WA
    University of Chicago School of Medicine, Chicago, IL

  • Related Resources

    • Mirzaa Lab

      Mirzaa Lab

      Dr. Ghayda Mirzaa is pinpointing the genes that contribute to many neurodevelopmental disorders. She helped discover many genes that cause focal cortical dysplasia, megalencephaly and microcephaly. This work is opening the door to new treatments that could modify or fix the errors in these genes, addressing the underly

  • Patient Testimonials

  • Awards and Honors

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  • Publications

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  • Presentations

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