Taking too long? Close loading screen.
CAMK2A

Welcome

This website provides information on patients with mutations in the CAMK2A gene, including clinical data, molecular data, management and research options. .

The syndrome caused by mutations in the CAMK2A gene is called autosomal dominant 53 mental retardation (OMIM # 617798). It is a multisystem disorder characterized by global developmental delay with shared characteristics including mild to severe intellectual disability, motor and speech delay, frequently associated with behavioural problems and possible seizures. Not all individuals with a mutation in the CAMK2A 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 CAMK2A gene.

Sébastien Küry, D.V.M., Ph.D., CHU de Nantes, Service de Génétique Médicale, 9 quai Moncousu, 44093, Nantes, France, sebastien.kury@chu-nantes.fr

Geeske van Woerden, Ph.D., Department of Neuroscience, Erasmus MC, P.O. Box 2040, NL-3000 CA, Rotterdam, The Netherlands, g.vanwoerden@erasmusmc.nl

Sandra Mercier, M.D., Ph.D., CHU de Nantes, Service de Génétique Médicale, 9 quai Moncousu, 44093, Nantes, France, sandra.mercier@chu-nantes.fr

To share and collect information about clinic management and research projects.

Clinical characteristics

Clinical characteristics

Click here

Upload clinical information (professionals)

Upload clinical information (professionals)

Click here

Upload clinical information (parents)

Upload clinical information (parents)

Click here