P102: KIF26A is mutated in the syndrome of congenital hydrocephalus with megacolon

• Mohammed Almannai,
• Lama AlAbdi,
• Sateesh Maddirevula,
• Maha Alotaibi,
• Bader AlSaleem,
• Yaser Aljadhai,
• Hessa Alsaif,
• Mussad Abu Khalid,
• Fowzan Alkuraya

Affiliations

Mohammed Almannai

Genetics and Precision Medicine Department, King Abdullah Specialized Children's Hospital, King Abdulaziz Medical City, Ministry of National Guard Health Affairs, Riyadh, Saudi Arabia

Lama AlAbdi

Department of Translational Genomics, Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia

Sateesh Maddirevula

Department of Translational Genomics, Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia

Maha Alotaibi

Children’s Hospital, King Saud Medical City, Saudi Arabia

Bader AlSaleem

Division of Pediatric Gastroenterology, Children's Specialized Hospital, King Fahad Medical City, Riyadh, Saudi Arabia

Yaser Aljadhai

Department of Neuroimaging and Intervention, Medical Imaging Administration, King Fahad Medical City, Riyadh, Saudi Arabia

Hessa Alsaif

Centre of Excellence for Biomedicine, Joint Centres of Excellence Program, King Abdulaziz City for Science and Technology (KACST), Riyadh, Saudi Arabia

Mussad Abu Khalid

Department of Neuroscience, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia

Fowzan Alkuraya

Department of Translational Genomics, Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia