Dr. Nagwa Meguid

Clinical Geneticist & Professor, National Research Centre (NRC), Cairo

Dr. Nagwa Meguid

Dr. Nagwa Meguid is an Egyptian clinical geneticist and professor at the National Research Centre (NRC) in Cairo. She specializes in neurodevelopmental disorders, particularly the genetic causes of autism spectrum disorder and fragile X syndrome, and has identified several novel genetic mutations and syndromes.

In 2002, she became the first Arab woman to receive the L’Oréal-UNESCO Award for Women in Science in the Mediterranean region. She established the Autistic Research Group and specialized clinics at the NRC to provide early diagnosis and intervention for children with special needs.

Dr. Meguid has also led public awareness initiatives addressing the risks of consanguineous marriages and continues to mentor emerging scientists while serving in international scientific advisory roles.

Professional Highlights : 

0 2002

L’Oréal-UNESCO Award Recipient

0 Founder

Autistic Research Group, NRC

0 Pioneer

Genetic Research in Autism & Fragile X

Dr. Nagwa Meguid Talk

Neurodevelopmental Conditions in Egypt

Abstract

This talk will explore the landscape of neurodevelopmental conditions in Egypt, focusing on prevalence, diagnostic challenges, and care pathways within local and regional contexts. Dr. Meguid will highlight clinical, genetic, and societal factors shaping outcomes for affected individuals and families, and discuss ongoing efforts to strengthen early detection, multidisciplinary care, and research capacity.

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Join a global community shaping the future of neurodevelopmental research, care, and advocacy.

Pharmacist, Scientist & Higher-Education Leader

Dr. Reem Olaby

Dr. Reem Olaby is a pharmacist, scientist, and higher-education leader actively engaged in curriculum reform, faculty development, and academic governance.

Her scholarly work focuses on the genetic, epigenetic, and proteomic underpinnings of neurodevelopmental and neurodegenerative disorders, including autism spectrum disorder (ASD), Fragile X syndrome (FXS), and Fragile X–associated tremor/ataxia syndrome (FXTAS).

She is dedicated to translating molecular research into impactful education strategies, clinical training initiatives, and interdisciplinary collaboration.

Research Focus : 

Neurodevelopmental Disorders

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