🐢🌊✨ Unique Flavour Alert! 🌊🐢 Phlur Beach Skin is here to bring your Minecraft adventures to life! 🥪 Details: [Link] #MinecraftObservable #RareSkin #TurtlePower 🐢🌊✨ Buy anything with 20% discount: cutt.ly/KrRd7W5Z
Genetic Testing for WHIM Syndrome: reducing barriers, proper panel analysis, and how to deal with variants of uncertain significance.
Learn more at checkrare.com/genetic-test...
#CheckRare #WHIMSyndrome #RareGenetic #RareAutoimmune #RareSkin
💡Rare Disease Spotlight: IgG4-RD
Learn more about this rare disease with our latest article checkrare.com/newly-approv...
#CheckRare #RareDisease #IgG4RD #RareAutoimmune #RareSkin
Rare Skin Conditions? New Hope! 🩺✨
Breakthrough treatments for uncommon skin disorders are here! From advanced diagnostics to cutting-edge therapies, find out how science is changing lives. 💡
#RareSkin #Dermatology #SkinHealth #MedicalBreakthroughs #Healthcare #SkinCare
We're so glad you shared this brilliant work at the #RareResearch25 Conference! A great example of progress and hope for #EBcare and #EBresearch in #RareSkin disease. Thank you for joining us and for everything you contribute to advancing rare disease research!
Based on results from a recent study in France, cSSC incidence seems to be higher in patients with Sézary syndrome than the general French population. cSSC appears to be more aggressive in patients and has a local recurrence rate of 13.1%.
Learn more at shorturl.at/vUzqi
#RareSkin #RareCancer
Generalized pustular psoriasis #GPP is a rare, severe form of psoriasis characterized by sterile pustules across large areas of skin.
Learn more on our Learning Page at checkrare.com/generalized-...
#CheckRare #GeneralizedPustularPsoriasis #RareSkin #RareDisease
A slide with a photo of the speakers and the title of the talk
🩹 Epidermolysis Bullosa Registry 🩹
Dr Sinéad Hickey (DEBRA Ireland) and Ms Lara Cutlar (NISR Solutions CLG) will share insights into the Epidermolysis Bullosa Registry, which is advancing care & research for those affected. #RareSkin
Join us! www.eventbrite.ie/e/...
Paula Ragan, President and Chief Executive Officer of X4 Pharmaceuticals, discusses the pathway of approval under the European Medicines Agency (EMA) for mavorixafor for patients with WHIM syndrome.
checkrare.com/ema-pathway-...
#CheckRare #RareDisease #RareGenetic #RareSkin
Jean Donadieu, MD, Service d’Hémato-Oncologie Pédiatrique, Hopital, Paris, provides an overview of WHIM syndrome.
Jean Donadieu, MD, Service d’Hémato-Oncologie Pédiatrique, Hopital, Paris, provides an overview of WHIM syndrome.
checkrare.com/whim-syndrom...
#CheckRare #RareDisease #RareGenetic #RareSkin #WHIM