The Saudi Rare Disease Summit taking place in Riyadh, KSA is the pioneering platform that will highlight rare diseases related to practice in pediatric neurology, in addition to metabolic and genetic close related disorders with neurological manifestation related to these diseases. The summit will provide you with comprehensive overview of critical issues. featuring interactive case studies, presentations and ample networking opportunities to discuss the main problems encountered during medical practice. Join Saudi Rare Disease Summit and be a part of this outstanding event for a remarkable learning and networking experience

Summit Chairman

Dr.-Ali-Al-Otaibi

 

 

Prof. Fahad Al Bashiri

Chairman, Pediatric Department, Professor, Consultant Pediatric Neurologist and Epileptologist, College of Medicine, King Khalid University Hospital, King Saud University, KSA, President, Saudi Pediatric Neurology Society, KSA

Scientific Committee

Prof. Fahad Al Bashiri

Prof. Fahad Al Bashiri

Chairman, Pediatric Department. Professor, Consultant Pediatric
Neurologist and Epileptologist, College of Medicine, King Khalid University Hospital, King Saud University, President, Saudi Pediatric Neurology Society, KSA
Dr. Khalid Hundallah

Dr. Khalid Hundallah

Consultant Pediatric Neurology, Assistant Professor, Prince Sultan Military Medical City, Deputy, Saudi Paediatric Neurology Society, KSA
Dr. Malak Alghamdi

Dr. Malak Alghamdi

Medical Geneticist, King Saud University Medical City, Head of medical genetic division, KSUMC, KSA
Dr. Musaad Abukhaled

Dr. Musaad Abukhaled

Consultant Pediatric Neurology, Epilepsy and Stroke, Section Head of Pediatric Neurology, King Faisal Specialist Hospital & Research Centre, KSA

Key Benefits of Attending

Identifying

innovative approaches to rare diseases diagnosis and management

Learning

from a team of outstanding regional and international experts about their recent research, achievements and powerful experiences in the field of rare diseases

Discussing

the most persistent clinical problems encountered during medical practice

Networking

with the entire key stakeholders and major players within the highly specialized healthcare
industry

Participating

in interactive sessions discussing cases of rare autoimmune disorders, rare diseases and methods of management

Key Topics

  • Duchenne Muscular Dystrophy
  • Pediatric Neurofibromatosis
  • Newborn Screening
  • Spinal Muscular Atrophy (SMA)
  • Rare disease Registry
  • Clinical Research in Rare Diseases
  • Genetic testing
  • Stem Cell Therapies for Rare Diseases
  • Gene Therapy

Registration Fees

Registration Type
Registration Fee
SPNS Member
SAR 200
Non-SPNS Member
SAR 400
Students and Nurses
SAR 150
Virtual Registration
SAR 1000
Vendors
USD 2000

Who should attend

Metabolic consultants,   Pediatricians,     Genetic consultants,    Pediatric Neurologists,       Molecular Geneticists,     Lab Technologists,     Neurologists,     General practitioner

PLATINUM SPONSORS

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GOLD SPONSOR

Bristol-Myers

SILVER SPONSOR

BRONZE SPONSORS

EXHIBITORS

ORGANIZED BY

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SUPPORTED BY

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MEDIA PARTNERS