#BardetBiedlSyndrome
I am happy my team obtained a collaborative grant with @cajaneklab.bsky.social from Czech Science Foundation to study #IFT, #kinesin KIF14 and #TubulinCode in #cilia and #BardetBiedlSyndrome @imgprague.bsky.social
November 28, 2025 at 7:32 AM
Today is the global Rare Disease Day 2026 and we together with colleagues from @imgprague.bsky.social want to raise awareness of research on rare diseases #ciliopathy #BardetBiedlSyndrome
February 28, 2026 at 1:43 PM
I am grateful for the opportunity to chat with Dr Stephen Johnston from A Race Against Blindness youtu.be/XUZMrMG4WKg?...
#raredisease #medsky #bardetbiedlsyndrome
Multispecialty care for BBS @ the Marshfield Clinic BBS Center of Excellence with Dr. Jeremy Pomeroy
YouTube video by A Race Against Blindness - Nonprofit Organization
youtu.be
April 7, 2025 at 12:53 AM
Tiny projections on the surface of human cells can determine whether we stay healthy or develop a genetic disorder. Cell biologist Helen May-Simera is an expert on the hair-like structures called #cilia 👉 www.magazine.uni-mainz.de/the-big-impa...

#CellBiology #MolecularBiology #BardetBiedlSyndrome
August 11, 2025 at 5:39 PM
Congratulations to Sindija Šmite for obtaining the funding from the Grant Agency of the @charlesuni.cuni.cz, & her co-worker Hanka Hajšmanová 🤩 🎉 Looking forward to the new discoveries in the amazing world of cilia biology in neuronal cell behavior #cilia #BardetBiedlSyndrome @imgprague.bsky.social
April 1, 2026 at 5:37 PM
February 18, 2026 at 8:12 PM
Our girl Izzie has been suffering from stage 4 kidney failure due to 2 rare genetic conditions that are attacking her kidneys. Kidney function is currently at 18%. We need to find a live donor asap. All expenses covered. #Kidney4Izzie #fsgsrarekidneydisease #bardetbiedlsyndrome #kidneytransplant
December 24, 2024 at 3:34 AM
An 18-year-old patient with #BardetBiedlSyndrome presented with blurry vision and reduced peripheral awareness.

Read the full case report here: https://bit.ly/4xKsdPA

#Optometry #RetinalDisease #GeneticDisorders
Optometry Dx: The Retinal Manifestations of Bardet-Biedl Syndrome
How can a patient’s history of Bardet-Biedl syndrome, a rare genetic condition, explain his visual blur and other eye and retina symptoms?
bit.ly
June 15, 2026 at 5:29 PM