As part of World Prader-Willi Syndrome Day, the Consorci Corporació Sanitària Parc Taulí is organizing an update session aimed at family members and caregivers.
Program of the session
9:00 a.m. Introduction, welcome and presentation of the program.
- Dr. Victor Martinez Director of the Genomic Medicine Center and coordinator of the Rare Diseases Unit, CCSPT.
- Mrs. Assumpta Mas. President of the SPW Catalonia Association
- Dr. Raquel Corripio. Director of the Department of Pediatrics and UEC coordinator of SPW, CCSPT. Coordinator of the Research Area in Rare Diseases of the Parc Taulí Institute for Research and Innovation (I3PT-CERCA).
- Dr. Assumpta Caixàs. Endocrinology and Nutrition Service. Head of SPW adults. Coordinator of the Obesity and SPW working group, and of the Metabolism and
Digestive in I3PT-CERCA. Coordinator of the SEEDO SPW working group, and of the SEEN genetic obesity working group.
Taulí 1. Advances in the medical field
Moderators: Dr. Raquel Corripio and Dr. Assumpta Caixàs
- 9:15 am – The Rare Diseases Unit. Ms. Núria Capdevila
- 9:30 am – Transition Day (from Pediatrics to Adults). Ms. Yolanda Couto
- 9:45 a.m. – Mental health continues to be a challenge. Dr. Susanna Esteba-Castillo
- 10:15 am – Psychotropic drugs in the SPW. Dr. Ramon Corona
- 10:30 a.m. – Colloquium
10:45 a.m. – Coffee break
Taulí 2. Progress in the scientific field
Moderators: Dr. Assumpta Caixàs and Dr. Raquel Corripio
- 11:15 am – Current clinical trials in Pediatrics. Dr. Raquel Corripio
- 11:30 am – Clinical trial with PBF-999 from Palobiofarma. Phase 2 results and phase 3 preparations. Dr. Assumpta Caixàs
- 11:45 a.m. – Colloquium
- 12:15 pm – Study of cognition in children. Dr. Lorena Joga
- 12:30 pm – Results of the study with proprioceptive blankets. Ms. Rocío Pareja
- 12:45 pm – Results of the pharmacogenetic study. Dr. Snow Baena
- 13:00 pm – Results of the neuroimaging study. Mr. Alex Moreno
- 13:15 p.m. – Ongoing study on thermogenesis. Dr. Alba Hernández
- 13:30 p.m. Colloquium
14:00 p.m. – End of the day
family members and caregivers of users with Prader-Willi Syndrome
