Ciliopathy Alliance

Ciliopathy Alliance The global voice of everyone affected by ciliopathies

The Ciliopathy Alliance is an alliance of medical researchers, doctors and patient organisations representing patients and families suffering from ciliopathy diseases. Ciliopathy diseases are caused by defects in the function or structure of cilia, small hair-like protuberances, like antenna, found on the surface of virtually every cell in the human body. Once thought to be vestigial organs, defective cilia are now understood to underlie a number of devastating genetic conditions including:

Alstrom Syndrome, Laurence-Moon-Bardet-Biedl Syndrome, Nephronophthisis, Orofaciodigital Syndrome, Polycystic Kidney Disease, Primary Ciliary Dyskinesia, Senior-Loken Syndrome, Usher Syndrome. The Alliance was formed to:

•Share knowledge and understanding
•Promote awareness of ciliopathies and the respective patient organizations
•Encourage collaborative research and facilitate where possible
•Apply for research funding from government, trusts and foundations

Do you have PCD? Are you part of the Living with PCD study? A new questionnaire on social functioning has just been sent...
01/12/2025

Do you have PCD? Are you part of the Living with PCD study? A new questionnaire on social functioning has just been sent out! Look out for it or sign up here

You can find latest news from the Living with PCD study here. Living with PCD (formerly COVID-PCD) is a research study that aims to answer emerging questions about primary ciliary dyskinesia (PCD).

Did you know that you can fundraise for us? All donations and fundraising helps support our mission to improve the lives...
01/12/2025

Did you know that you can fundraise for us? All donations and fundraising helps support our mission to improve the lives of people affected by ciliopathies.

26/11/2025

We are delighted that https://www.facebook.com/heterotaxyconnection have joined our alliance and we look forward to collaborating with them.

Heterotaxy Connection is a nonprofit supporting individuals and families affected by heterotaxy syndrome. We provide education, advocacy, and community connections to improve awareness, care, and outcomes

21/11/2025

A team of researchers from the University of Edinburgh is working to better understand the genetic basis of rare conditions. Their new project will investigate the underlying genetic mechanisms of rare conditions and explore possible links between different disorders that may be more closely related than people realise. By deepening this understanding, they hope to improve genetic testing and expand treatment options for those affected.
To ensure the research reflects the priorities and experiences of the rare disease community, they're hosting an online focus group to hear people’s views.

The session is open to anyone living with a rare disease, as well as primary carers. They are particularly keen to hear from people both with and without a confirmed genetic diagnosis — including those still seeking one or whose condition has been categorised as a Syndrome Without a Name (SWAN).

The focus group will last 90 minutes and will take place online via Zoom. Take part here: https://forms.cloud.microsoft/pages/responsepage.aspx?id=sAafLmkWiUWHiRCgaTTcYSEz2ebJYdZMjDYA6mceYfRURDRRQTAyVEMyREdaWTBST1pVQzE5RU4xTC4u&route=shorturl

Do you have financial experience and an interest in Ciliopathies? We are looking for a new treasurer to join our board o...
20/11/2025

Do you have financial experience and an interest in Ciliopathies? We are looking for a new treasurer to join our board of trustees. Please contact us for more information or if you thin you may be able to help.

We are looking for a treasurer to join our board of trustees to help us achieve our short-term goals and to ensure the long-term viability of the alliance. To do this we believe an enthusiastic treasurer with great communication skills, experience of working in financial management and some knowledg...

Update from Ciliopathy Alliance November 2025 -
05/11/2025

Update from Ciliopathy Alliance November 2025 -

We have had a very busy few months at the Ciliopathy Alliance - taking on some volunteers to help us (thank you to Adrian for writing the profile on Fiona’s Honorary Doctorate and writing a volunteer policy) and Hannah who has helped us review some policies. We have also taken on three interns fro...

We hosted a great webinar today about skeletal ciliopathies, genetic diagnosis and the importance of getting support fro...
26/09/2025

We hosted a great webinar today about skeletal ciliopathies, genetic diagnosis and the importance of getting support from Retina UK today.

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....

Thanks Kerry and Alström Syndrome UK
22/09/2025

Thanks Kerry and Alström Syndrome UK

Today, our Chief Executive Kerry Leeson-Beevers is presenting on behalf of the Ciliopathy Alliance at the TheRaCil Project: Advancing Therapies for Paediatric Renal Ciliopathies Annual Meeting.

Alstrom Syndrome Alstrom Syndrome International Alstrom Syndrome Canada Initiative Alström ASSAI APS - Associazione Sindrome di Alström Italia Síndrome de Alström España Alström sindrom-Hrvatska

You can find out more about their work on their website:
https://theracil.eu/

Lovely day in London meeting potential volunteers
28/07/2025

Lovely day in London meeting potential volunteers

Our Treasurer Temi attended her first scientific cilia meeting last week ... here are her reflections.
25/06/2025

Our Treasurer Temi attended her first scientific cilia meeting last week ... here are her reflections.

On Friday, 20th June 2025 - some of our Trustees attended the UK Cilia and Centrosome Network Meeting which was hosted by Hannah Mitchison our Chair. Thanks to Kerry Leeson-Beavers for updating the group about the CAUK's strategy.

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