Molecular basis of several congenital or neonatal endocrine disorders and establishment of new therapeutic strategies

Our  goal is to study some rare forms of congenital disorders of the endocrine pancreas.

In the last fifteen years, we have focused our research on some specific forms of neonatal diabetes in Human. We have been able to define innovative treatments for children with neonatal diabetes, a rare genetic form of dysfunction of the insulin-secreting cell.

During those years we have gained a considerable experience in the study of the molecular control of the  islet cell development and we have also been able to establish a network with clinicians from France, Europe and several other countries in particular from Maghreb and Middle east; through this collaboration a depository of rare disorders of the endocrine pancreas has been established with a precise description of cases and DNA from index cases. This is a very helpful biological resource to continue our work.

Our team intends to pursue this « translational » research through further clinical trials, in link with our pediatric endocrinology and diabetology department at Necker Enfants Malades hospital and the clinical investigation center within Institut Imagine. We believe that, through the discovery of new molecular anomalies of endocrine pancreas development we will :

• better understand some aspects of the development of those glands
• discover some anomalies, which are observed much more frequently in adults in an heterozygote state