Rare Disease Medical Animations

Cinematic productions on rare diseases, meticulously crafted to be medically accurate and deeply engaging.

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FABRY DISEASE PATHOPHYSIOLOGY: VISUALIZING ALPHA-GAL DEFICIENCY AND GL-3 STORAGE

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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.

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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

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

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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.

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Contact

Please contact us using the details below.

Office

410, Highgate Studios,
53-79 Highgate Road,
London NW5 1TL0

T +44 (0)207 127 6935

+44 (0)207 127 6935

M +44 (0)7970 080 690

+44 (0)7970 080 690

info@fusionanimation.co.uk

info@fusionanimation.co.uk

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