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16th National Research Competition in Life and Earth Sciences
Rare diseases
Research Centre or Institution : Fundación Pública Gallega de Medicina Genómica. Santiago de Compostela.
The overall aim of this project is to identify all Spanish patients with congenital autosomal recessive icthyosis (ICAR), as well as to characterise them clinically and genetically. The project started in June, 2012. During these months, the group has concentrated on publicising the project with the objective of identifying the Spanish patients involved, including them in the protocol and studying a new gene associated with the disease (PNPLA1).
A new gene, PNPLA1, was recently identified as causing ICAR (Grall et al., 2012). This gene was studied in the families of Galician patients without mutations in the TGM1, ALOXE3, ALOX12B, NIPAL4, CYP4F22 and ABCA12 genes. One of these families presents an alteration in the homozygosis of this gene. A sample has been requested from the brothers of the patient (healthy and affected) to discover the involvement of the variant of the disease that has been identified.
Activities related
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Publications related
International Symposium Understanding and reprogramming developmental visual disorders: from anophthalmia to cortical impairments Madrid, Thursday and Friday, 30 and 31 January 2020, 9:30 hours
Panel Discussion Mundo de las prótesis, los nuevos materiales, sus complicaciones y su futuro Madrid , Lunes, 8 de abril 2024. 17.00 horas
Session Situación actual de las Enfermedades Raras en España Madrid, Martes, 23 de abril de 2024, 10:00 horas


La Fundación Ramón Areces refuerza su compromiso con las enfermedades raras
Published on 04/23/2024