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Cystinosis is a rare, metabolic disease characterised by a build up of the amino acid, cystine, in organs and tissues, leading to severe organ dysfunction. In Cystinosis, the transporter for cystine is dysfunctional, causing a build up of cystine in the cells which then crystallise.

What Does it do?

The crystals quickly create toxic levels of cystine in the body, causing cellular dysfunction and even cellular death. Soft tissue and all organs are directly affected by this crystallisation, including the kidneys, eyes, liver, muscles, and central nervous system.

What Can we Do?

Cystinosis Ireland provides support and resources to families, medical professionals, researchers and others from the early stages of diagnosis through to adulthood.

Research

We back global cutting-edge Cystinosis research, collaborating with DNA and Stem Cell experts, making us a prominent partner in the global fight for a cure.

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Awareness

We hold events and fundraisers to support individuals and families affected by Cystinosis, addressing immediate needs and advancing future research.

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Support

One of the most important aspects of Cystinosis Ireland is that we provide a community of support and knowledge to every family impacted by Cystinosis.

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Latest News

News, Events 10/04/2025

Cystinosis Ireland to host 2026 international conference

Save the date for the 2026 CNE International Conferee in Dublin!

News, Research 04/04/2025

Now enrolling: Phase I/II CYStem clinical trial

News 03/03/2025

Rare Diseases Day 2025