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We want to improve the lives of children and adults affected by ciliopathies - syndromes, diseases or conditions caused by dysfunctional or defective cilia.

We want to improve the lives of children and adults affected by ciliopathies - syndromes, diseases or conditions caused by dysfunctional or defective cilia.

Welcome to the Ciliopathy Alliance

The Ciliopathy Alliance brings together patient support groups, researchers, doctors and allied health professionals representing patients and families living with and affected by ciliopathies- diseases caused by defects in the function or structure of cilia.

Dysfunctional cilia are known to underlie a number of often chronically disabling and sometimes life-threatening genetic conditions. They affect multiple systems, causingblindness, deafness, chronic respiratory infections, kidney disease, heart disease, infertility, obesity and diabetes.

Over 20 ciliopathies have been identified and more are suspected, with an estimated 1 in 1,000 people affected.

Our shared vision is to improve the quality of life for people living with ciliopathy syndromes and conditions. Please join us in this endeavour.

Recent News

Webinar on Skeletal Ciliopathies, Genetic Diagnosis and Support Groups

Webinar on Skeletal Ciliopathies, Genetic Diagnosis and Support Groups

26 September 2025

On Friday, 26th September we hosted the 3rd Webinar on Skeletal Ciliopathies, Genetic Diagnosis, and Support Groups.

Rhoda Akilapa, Consultant in Clinical Genetics at Guy's and St Thomas' NHS Foundation Trust gave an insightful presentation on skeletal ciliopathies and how they are diagnosed. Matthew Carr, Special Projects Manager from Retina UK told us about the work of the charity who are celebrating their 50th Anniversary this year and the role of support groups in supporting patients after a genetic diagnosis. Fiona Copeland finished the meeting discussing how the Ciliopathy Alliance can support patients where there are no established support groups.

To watch the webinar click here

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