This website provides information on patients with mutations in the WDR4gene, including clinical data, molecular data, management and research options.
Disorders caused by mutations in the WDR4gene include the following: Galloway-Mowat syndrome 6 (GAMOS6) and WDR4-related Microcephaly, growth deficiency, seizures, and brain malformations (MIGSB). Both disorders follow an autosomal recessive inheritance pattern
Not all individuals with a mutation in the WDR4gene have these features.
This website was created to share and collect information about clinic, management and research projects to gather more knowledge and provide better treatment of patients with mutations in the WDR4gene.
Fowzan S. Alkuraya, MD (Hons) ABP ABMG, Department of Translational Genomics, Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia, falkuraya@liferaomics.com.sa
Khadijah Bakur, PhD, Lifera Omics, Riyadh, Saudi Arabia, kbakur@liferaomics.com.sa