Research and Hope for LAL-D

Research and Hope for LAL-D

  New Research Project Explores Innovative Strategies for Lysosomal Acid Lipase Deficiency (LAL-D) At LAL-D Patient Organization, we would like to congratulate Matthias Zadory on the successful defense of his doctoral thesis, “Engineering Non-Viral Gene...
“Lipids and Health” Conference

“Lipids and Health” Conference

“Lipids and Health” Conference: Early Diagnosis, Multidisciplinary Care and Access to Treatment https://lald.org/wp-content/uploads/2026/07/Jornada-Lipidos-y-Salud.mp4   On June 30, the Faculty of Medicine of the University of Barcelona hosted the “Lipids and...
LAL-D: much more than a rare disease

LAL-D: much more than a rare disease

A new publication in Hepatology International provides important evidence about the role of lysosomal acid lipase (LAL) in liver disease progression. The study shows that lower LAL activity is associated with: 👉 Increased liver inflammation 👉 Greater fibrosis...
The FC Barcelona Foundation supporting Rare Diseases

The FC Barcelona Foundation supporting Rare Diseases

Martina, affected by LAL-D, represented the LAL-D Patient Organization at the event On the occasion of World Rare Disease Day, the FC Barcelona Foundation made it possible for girls affected by rare diseases to experience a truly unforgettable day alongside the...
Rare Disease Day

Rare Disease Day

RARE DISEASE DAY 2026 February 28th marks Rare Disease Day. Early diagnosis can change a life. High cholesterol is very common in the population. However, in some cases it may be a sign of a rare condition such as lysosomal acid lipase deficiency (LAL‑D). If you have:...