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  1. La identificación del gen responsable de una enfermedad es el primer paso para el mejor entendimiento de su patofisiología lo que a su vez supone el punto de partida en el desarrollo de dianas terapéuticas. El proyecto se inició en 2011 tras el contacto entre Carles (presidente de la Asociación de Pacientes de Opitz C y padre Marta, una paciente) y nuestro grupo de Genética Molecular Humana de la Universitat de Barcelona (liderado por los Drs. La historia de Carles y su familia y lo devastador de este síndrome nos conmovió y decidimos asumir el reto de buscar el gen o genes responsables de este síndrome.