Seminar "Rare hereditary childhood cancer syndromes"

The seminar "Rare hereditary childhood cancer syndromes" will address six main genetic disease - von Hippel-Lindau syndrome, Li-Fraumeni syndrome, Multiple endocrine neoplasias syndromes (MEN1 and MEN2), Familial adenomatous polyposis and Type 2 Neurofibromatosis - which can manifest in childhood and young age.

The targeted audience are clinicians and scientists, working with patients suffering from hereditary cancer predisposition disoroders.

This seminar is a part of ongoing academic research project "National hereditary childhood cancer research platform" jointly supported by European Economic Area (EEA) & Norwegian Financial Mechanisms scheme and Vilnius university hospital Santariskiu clinics.

More information: http://pvas.lt/Naujienos.php