📌L’ @istsupsan ISTITUTO SUPERIORE SANITÀ organizza un corso di formazione sulle malattie rare non diagnosticate.
Il corso dal titolo “Training on strategies to foster solutions of undiagnosed #raredisease cases”, si svolgerà online e in lingua inglese dal 12 al 14/04
27 – 29 April 2020. This workshop is now online with a web-conferencing format. The program has been adapted.
Due to the force majeure situation, the international travel policies associated with COVID-19 and extraordinary measures to limit the spread of the virus, the Italian health authorities (including the Istituto Superiore di Sanità, ISS), recommend adopting a precaution approach and cancel the planned trips and events. In order to ensure the correct progress of the planned tasks of EJP RD, ISS ensures that the international course “Training on strategies to foster solutions of undiagnosed rare disease cases”, 27-29 April 2020, ISS, Rome will be held ONLINE.
Participants who have been selected to attend the course will be informed of the means and tools for using the online version of the training course.
INTRODUCTION AND OBJECTIVES
The International Course Training on strategies to foster solutions of undiagnosed rare disease cases is part of a series of training activities proposed by the EJP RD. EJP RD is a European Commission funded project (grant agreement No 825575, 2019 – 2023) with the goal “to create a comprehensive, sustainable ecosystem allowing a virtuous circle between research, care and medical innovation”.
This International course is part of WP14 of the EJP RD, “Training on Data Management & Quality”; Task 14.3 “Training on strategies to foster solutions of undiagnosed rare disease cases”. WP and Task Leader: Dr. Claudio Carta, ISS.
Course Director: Dr. Domenica Taruscio, ISS.
The Course is made up of 3 days of residential training organized by ISS, Istituto Superiore di Sanità, in close collaboration with EJP RD task partners: EKUT, LBG (LBI-RUD) –Ludwig Boltzmann Gesellschaft GMBH, Vienna, Austria; ACU/ACURARE – Acibadem Universitesi, Istanbul, Turkey; ISCIII – Instituto de Salud Carlos III, Madrid, Spain; INSERM (AMU) Institut National de la Santé et de la Recherche Medicale, Marseilles, France; FTELEFondazione Telethon, Milan, Italy; UMCGAcademisch Ziekenhuis Groningen, Netherlands; IMAGINE Imagine Institut des Maladies Genetiques Necker Enfants Malades, Fondation, Paris, France; CNAG-CRGFundacio Centre de Regulacio Genomica, Barcelona, Spain; IPCZD (CMHI) – Instytut Pomnik Centrum Zdrowia Dziecka, Warsaw, Poland, and with the endorsement of ICORDInternational Conference On Rare Diseases and Orphan Drugs.
Several initiatives have been undertaken at national and international level for undiagnosed rare diseases aimed at identifying clinical pathways and innovative methods to reach diagnosis. This course will illustrate methodologies and tools already used internationally and will provide participants with useful examples for the resolution of undiagnosed cases.
The course will provide participants, through the presentation of sample use cases that have long eluded diagnosis, with useful tools, instruments and knowledge on novel strategies to foster solutions of undiagnosed RD cases. Moreover, the course will facilitate networking among professionals involved in undiagnosed rare conditions.
The first two days will be dedicated to plenary presentations and Problem-Based Learning (PBL). PBL is a highly interactive and learner-centred approach in which participants, working in small groups assisted by a facilitator, find the solution to a problem that will be discussed at the end of the session with the experts. On the third day of the course, a hands-on experience with practical demonstrations of useful bio-informatics resources will be shown to the participants.
Participants are asked to bring their laptops for the PBL and the practical demonstration sessions.
The International course is open to the international research community, to clinicians and to medical specialists who have experience and concrete interest in the diagnosis and research of Rare Diseases.
To ensure active participation and exchange with teaching staff and participants, a maximum of 30 attendees will be admitted. A selection process will be applied based on the participants’ background in: genotypic and/or phenotypical identification of rare disorders; deep phenotyping; inferring variants; digital technologies in rare diseases. Priority will be given to participants involved in national and international Rare Disease Programs and Projects: Undiagnosed Diseases Network International (UDNI), Solving the Unsolved Rare Diseases (Solve-RD), and the European Reference Networks (ERNs).
This course foresees four fellowships for participants resident, living and working in an EU13 Country (Bulgaria, Croatia, Cyprus, Czech Republic, Estonia, Hungary, Latvia, Lithuania, Malta, Poland, Romania, Slovakia, Slovenia). For more information about eligibility and criteria for selection, contact Claudio Carta at: claudio.carta(at)iss.it
For each fellowship a maximum of 350 euros for travel (flight and/or train round trip) and 120 euros/night for hotel accommodation for a maximum of 3 nights is available.
Registration is closed.
FEES AND COSTS
The course and the registration are free of charge. Coffee, refreshments and lunches will be offered during the course. Travel, accommodation and other costs incurred to attend the course are at the expense of the participants. The course organisers will not cover expenses incurred by the participants in any case.
Group presentations are foreseen to assess the new learning. A satisfaction questionnaire will also be submitted to the participants.
At the end of the course a certificate of attendance will be handed to the participants who attended 100% of the course. No credits of Continuing Education in Medicine will be issued.
Workshops will run in English.
If you have questions please write to the course organiser Claudio Carta, PhD: