This website provides information on patients with mutations in the LMNB1 gene, including clinical data, molecular data, management and research options.

The syndrome caused by mutations in the LMNB1 gene is a multisystem disorder characterized by microcephaly, intellectual disability of variable degree, growth retardation and seizures. Not all individuals with a mutation in the LMNB1 gene 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 LMNB1 gene.

Hilde Van Esch, MD, PhD, Center for Human Genetics, University Hospitals UZ Leuven, Leuven, Belgium, Hilde.VanEsch@uzleuven.be

Rich Steet, PhD, JC Self Research Institute, Greenwood Genetic Center, Greenwood, USA, rsteet@ggc.org