Reflection Biotechnologies (ReflectionBio) is a patient-driven biotech company focused on developing #GeneTherapy for rare retinal diseases.

Patients are global
Joined March 2018
Are you an RP patient? Do you have crystals in the retina? If so, you may have Bietti’s Crystalline Dystrophy (BCD). BCD is an autosomal recessive #RetinitisPigmentosa (RP) caused by mutations in the CYP4V2 gene. Potential treatments are being developed for BCD. @Invisionbcd
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#BiettiCrystallineDystrophy (BCD) worldwide genetic prevalence. This in-depth study published in TVST @ARVOtvst estimates that there are 67,000 BCD patients worldwide. This study was a collaboration between Dr. Dror Sharon and ReflectionBio. doi.org/10.1167/tvst.12.2.27
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ReflectionBio - By Patients, For Patients retweeted
Life is full of silver linings. One of those silver linings is the progress that @reflectionbio is making in gene therapy. Make this silver lining a little brighter by donating to Invincible Vision! invinciblevision.org/fundrai… #InternationalWomensDay #womenshealth #womensday2021
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We are proud to partner with @Invisionbcd in the BY PATIENTS, FOR PATIENTS ™ campaign for #BiettiCrystallineDystrophy (BCD). BCD is a rare blinding disease. It is often misdiagnosed as #RetinitisPigmentosa (RP) or Stargardt Disease. youtu.be/eFogU2bfxcw
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A cool way to explain ocular #GeneTherapy
Here is my latest animation on #GeneTherapy for Genetic Eye Diseases. It explains the principles in simplified way. Thanks to Charlotte Patten @MoorfieldsBRC and @swing4cat for their technical skills! Hope you ❤️ it! vimeo.com/459289004
ReflectionBio is proud to be part of the Orphan Drug Development Guidebook Task Force @IRDiRC. We are grateful for the opportunity to work closely with such a diverse group of orphan drug experts from different parts of the world. #RareDiseases #OrphanDrug
🆕 appointment of the #irdirc Orphan Drug Development Guidebook, today we discover the Technical Experts Affiliations that have work on this important project! Thank you! 👉irdirc.org/activities/task-f… #rarediseases @SanRaffaeleMI @LeuvenU @Roche
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BCD Misdiagnosis 2: The clinical symptoms and findings on visual field testing and electrophysiologic studies in Bietti Crystalline Dystrophy #BCD are similar to those of other forms of retinal degeneration including Retinitis Pigmentosa (RP). ncbi.nlm.nih.gov/books/NBK91…
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It is estimated that there are more than 100,000 patients in the world suffer from #BCD, i.e., have crystals in their eyes. @invisionbcd
‘Crystals in my eyes’ .. sounds beautiful and rare - true!! But also a symptom of #BiettisCrystallineDystrophy #BCD is a very rare blinding eye disease, often misdiagnosed. #goingblind #retina #opthamologist #nocyee #bcdawareness #invinciblevisionorg
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ReflectionBio - By Patients, For Patients retweeted
If you're worried about attending your appointment at Moorfields, read through Cilla's story on how she has been reassured by the measures we have taken to make sure our patients and staff stay safe during these times.
Like many, Cilla was worried about attending her eye clinic when the coronavirus outbreak began and was relieved when her appointment was postponed. But when her sight started to deteriorate she knew she had no choice @Moorfields macularsociety.org/news/thou…
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In difficult times like the COVID-19 pandemic we are facing now, we should be mindful that it creates unique challenges for people with disabilities. This includes many #RareDiseasePatients. They also need help and should not be neglected. @PatientWorthy
COVID-19 poses unique challenges for people with disabilities bit.ly/3eNh8EC via @HubJHU
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Diva on bietti's crystalline dystrophy (BCD). BCD is a blinding disease. Patients have yellow-white crystals in the retina. It is caused by mutations in the CYP4V2 gene. Currently, BCD is untreatable. ReflectionBio is developing BCD gene therapy. youtu.be/FS4jCA5S2DU
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Congrats to the Orphan Drug Development Guidebook Task Force of #IRDiRC on this #OrphanDrugDevelopment paper. ReflectionBio's founder & CEO is honoured to serve on this IRDiRC Task Force as an orphan drug developer and a rare disease patient. #ByPatientsForPatients
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Great Initiative for patients suffering from Inherited Retinal Diseases (IRDs)! Given there are 200+ IRDs, genetic testing is important for the correct/precise diagnosis of IRDs.
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Thank you, Laurel, for sharing your experience living with #BiettiCrystallineDystrophy (BCD), a rare blinding disease. As a patient-driven biotech company, we are proud to hear that our efforts in developing #BCD #GeneTherapy bring hope to the patient community.
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ReflectionBio - By Patients, For Patients retweeted
#GeneTherapy #Luxturna (voretigene neparvovec) has been recommended for reimbursement by the UK's National Institute for Health and Care Excellence @NICEComms for the treatment of a specific type of #LCA, an Inherited Retinal Disease #IRD bbc.com/news/health-49565740…
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