This Fusion Animation for patients and carers uses 3D medical animation to illustrate the Pathophysiology and Mechanism of Disease (MOD) for Fabry disease, a genetic lysosomal storage disorder. We visualize the core defect: a missing alpha-GAL enzyme. This deficiency causes the toxic, progressive accumulation of the fatty substance GL-3 within cells and organs, leading to severe organ damage. This showcases our expertise in visualizing complex concepts in Rare Genetic Diseases.
Rare Disease Medical Animations
Cinematic productions on rare diseases, meticulously crafted to be medically accurate and deeply engaging.

FABRY DISEASE PATHOPHYSIOLOGY: VISUALIZING ALPHA-GAL DEFICIENCY AND GL-3 STORAGE
This Fusion Animation for patients and carers uses 3D medical animation to illustrate the Pathophysiology and Mechanism of Disease (MOD) for Fabry disease, a genetic lysosomal storage disorder. We visualize the core defect: a missing alpha-GAL enzyme. This deficiency causes the toxic, progressive accumulation of the fatty substance GL-3 within cells and organs, leading to severe organ damage. This showcases our expertise in visualizing complex concepts in Rare Genetic Diseases.

Bardet-Biedl syndrome
Brief: Explain how BBS affects the body, in a way suitable for young patients, families, and carers—with consideration for vision impairments.






