Manchester Rare Conditions Centre
@mft_iMRare
Official Manchester Rare Conditions Centre account. Improving lives of people with rare conditions
We're pleased to announce the launch of a RDCN for individuals with Ectodermal Dysplasia (ED) & related conditions. The RDCN brings together a group of expert providers committed to improving patient care, advancing research & increasing awareness. rb.gy/ee7u1w
⏳LAST CHANCE! ⏳ #MDC2025 #RARECONDITIONS Abstract submissions for #Dysmorphology2025 close TOMORROW at Midnight BST! 🔗 Submit here: mrcc.org.uk/events/confere… Tag someone who needs to see this! 👇 📝
📰 Two groundbreaking genetic discoveries from Manchester BRC could provide answers for thousands of people with neurodevelopmental conditions globally. Rose from Manchester received a diagnosis of one of the newly discovered conditions after 18 years 👇 manchesterbrc.nihr.ac.uk/news-and-event…
Thank you @AlexionPharma for inviting the MRCC to The Rare Network Innovation Exchange! Dinesh Chawla, MRCC Manager, will be taking part in the exchange, discussing strategic frameworks to improve the sustainability and impact of rare disease services.



May was a fantastic month for seminars at the MRCC.Thank you to our wonderful speakers Chris Smith,Prof Radick & Dr Grzechnik for your fascinating presentations.Interested in attending our seminars?We'll share the program for future seminars on our website:shorturl.at/uT5P4



MDC 2025 Abstract Deadline Extended! We have extended the submission deadline to Tuesday 10th June! Remember you must have an abstract accepted to be able attend 20th Manchester Dysmorphology and Developmental Disorders Conference 16th-19th Nov 2025 mrcc.org.uk/events/confere…
Ever heard of CLCN4-related disorder? It’s a rare condition caused by CLCN4 gene changes. In May, Kamal joined the Cure CLCN4 Conference in London-an event bringing together experts & families to drive research & treatments. 👉 cureclcn4.org 👉 lnkd.in/eGDKcVEk
In 2023, 252 genomics experts from 50 countries attended MDC.Clara Tang,Director of Research @kabukisyndrome shared that “it was a great chance to learn & connect with passionate clinicians and researchers focused on rare conditions like Kabuki syndrome.” shorturl.at/TsHSo

📢Clinicians: This is your last chance to lead the development of new Unique Information Guides for rare genetic neurodevelopmental disorders using a cutting-edge AI solution. Final deadline: 6ᵗʰ June. Submit your proposal here: forms.office.com/e/jziupyz04f 🔗mrcc.org.uk/news/2994/

Listen to experts who attended the Manchester Dysmorphology and Developmental Disorders (MDC) Conference 2023 lnkd.in/eixFCUhP Remember you must have an abstract accepted to be able attend 20th MDC 16th-19th Nov 2025 lnkd.in/eP9pZy3Y
MDC @Ddysmo reflects,"MDC 23 was everything we hoped for in 1984—international, engaging, & full of insights into rare conditions.The complexity & emerging treatments exceeded expectations. I’m confident #MDC2025 will surpass it!"Submit your abstract here shorturl.at/w5Fw0
📢Abstract submission is OPEN for the 20th Manchester Dysmorphology & Developmental Disorders Conference (MDC)! Browse past programmes & go on a journey through the history of #MedicalGenetics here: lnkd.in/ed9aKU7H Deadline: 6th June Submit here: shorturl.at/0SSY8
We are calling clinicians to propose rare genetic neurodevelopmental disorders, which they will be willing to lead development of a new guide, with assistance of our generative AI model. Propose a condition by 30th May: forms.office.com/e/jziupyz04f @nwgmsa @mft_iMRare
📢 This months free educational seminar series invites specialist speakers from University of Leeds and @OfficialUoM to join us at @MFTnhs Interested in attending? Email [email protected] to find out how.

Thank you Dr Anna Shawcross for your fascinating talk on Cystic Fibrosis - Times Have Changed! If you're interested in learning more, check out the following paper: sciencedirect.com/science/articl…

📣 We translate scientific discoveries into new tests, treatments and preventative measures to improve lives and reduce health inequalities. Find out how our Rheumatic and Musculoskeletal Diseases Theme is reducing health inequalities through research 👇 manchesterbrc.nihr.ac.uk/our-research/r…
We are so happy to receive such positive feedback from participants who took part in the @eshgsociety European Society of Human Genetics course on Cardiac Genetics in Manchester this year. Thank you to all for sharing your expertise, knowledge and passion. @GeneticBill

That's a wrap! 1st @EpiGenRare @RDRUK_ELSI @REOLUT conferences are over.A big shout to our amazing organisers, Gabrielle Parkinson & Henry Frost & dream support team Hannah Jackson & Eva Clarke for making this happen! Thanks to all inc patients & families @RDRUKHub @OfficialUoM

