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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, Research 19/11/2024

Article: Patient journey in cystinosis: focus on non-adherence and disease management

News 30/10/2024

Novartis Community Statement October 2024

News 30/10/2024

Budget 2025 changes for carers