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The EURO-WABB Project

An EU Rare Diseases Registry for Wolfram syndrome, Alström syndrome, Bardet-Biedl syndrome and other rare diabetes syndromes.

Breadcrumbs

Update to the Alstrom Syndrome Clinical Utility Gene Card

The Clinical Utility Gene Card for Alstrom syndrome which was first published in 2011. Click HERE to read

Euro-WABB Recruitment Exceeds 200 Participants!

More than 200 participants are now taking part in the Euro-WABB registry project.

Congratulations to Euro-WABB Associate Partners!

The Euro-WABB Team would like to congratulate two of the project's Associate Partners, Prof. Ségolène Aymé and Kay Parkinson, whose work outside of Euro-WABB was recognised during the recent EURORDIS awards ceremony. Prof. Ségolène Aymé received the Scientific Award and Kay's Charity, Alström Syndrome UK, were awarded the EURORDIS Patient Organisation Award.

Natural History of Wolfram Syndrome Paper Published

Researchers at IDIBELL and CIBER de Enfermedades Raras (CIBERER), Spain, have recently published in the Genetics in Medicine journal. The research updates the natural history of Wolfram syndrome, provides some clues to understand the different clinical outcomes between patients, and estimates the progression of the disease, by collecting the data from 400 patients published world-wide during the last 15 years. You access the abstract HERE

New Journal Article about Wolfram Syndrome Published

Researchers at the University of Birmingham, UK have recently published findings from their laboratory research in the Human Molecular Genetics journal. The research shows how cells cannot release their cargoes of proteins into the bloodstream. It is because the Wolfram protein has to interact with an enzyme that makes the inside of the protein packets acid, without which they cannot dock with the cell membrane. You can read a simplified summary of the research HERE, or access the abstract HERE.