We are pleased to share that Leticia Pías Peleteiro, MD, and Encarna Guillén Navarro, MD, PhD, have joined the Scientific Advisory Board of POU3F3.org.
Dr. Pías Peleteiro is a neuropediatrician at Hospital Sant Joan de Déu Barcelona with expertise in genetics and rare diseases. She brings direct clinical experience caring for children with complex neurodevelopmental and genetic conditions, adding valuable perspective to our work to support children and families affected by Snijders Blok-Fisher syndrome and other POU3F3-related conditions.
Dr. Guillén Navarro is a pediatrician and medical geneticist who serves as Head of the Genetics Area and Strategic Director of Únicas SJD at Hospital Sant Joan de Déu Barcelona. She leads work in genomic medicine and rare diseases and brings deep experience in clinical genetics, translational research, and rare-disease strategy that strengthens our foundation’s scientific direction.
We are honored to welcome both of them and grateful for their willingness to contribute their time, knowledge, and guidance to this effort. Their involvement will help strengthen our organization’s scientific foundation as we work to support research, family resources, education, collaboration, and long-term progress toward meaningful therapies.
