Latest Global Clinical Trials for Retinitis Pigmentosa (2026 Update)Medically reviewed by Dr. Prashant Tyagi (Stem Cell Biotechnology Specialist, 10+ years) and Dr. Pallavee Senior Consultant | Ophthalmologist & Eye Surgeon 22+ Years Experience For patients and families living with retinitis pigmentosa (RP), staying informed about ongoing...
Medically reviewed by Dr. Prashant Tyagi (Stem Cell Biotechnology Specialist, 10+ years) and Dr. Pallavee Senior Consultant | Ophthalmologist & Eye Surgeon 22+ Years Experience One of the questions patients ask most often after an RP diagnosis is simply: what happens next, and how quickly? While...
Medically reviewed by Dr. Prashant Tyagi (Stem Cell Biotechnology Specialist, 10+ years) and Dr. Pallavee Senior Consultant | Ophthalmologist & Eye Surgeon 22+ Years Experience A confirmed retinitis pigmentosa (RP) diagnosis typically relies on two key tools working together - electroretinogram (ERG) testing and genetic testing....
Medically reviewed by Dr. Prashant Tyagi (Stem Cell Biotechnology Specialist, 10+ years) and Dr. Pallavee Senior Consultant | Ophthalmologist & Eye Surgeon 22+ Years Experience Patients researching treatment options for retinitis pigmentosa (RP) often come across two very different approaches - gene therapy and stem cell...
Medically reviewed by Dr. Prashant Tyagi (Stem Cell Biotechnology Specialist, 10+ years) and Dr. B. N. Singh (General Physician, MBBS MS General Surgery, 30+ years) For many patients later diagnosed with retinitis pigmentosa (RP), the earliest signs were dismissed for years - attributed to tiredness, poor...
Medically reviewed by Dr. Prashant Tyagi (Stem Cell Biotechnology Specialist, 10+ years) and Dr. Pallavee Senior Consultant | Ophthalmologist & Eye Surgeon 22+ Years Experience Retinitis pigmentosa (RP) is one of the most common inherited retinal conditions, yet many patients receive the diagnosis with very little...
Rod & Cone Dystrophy: Causes, Symptoms, Diagnosis, and Treatment Rod & Cone Dystrophy (RCD) is a rare inherited retinal disorder that affects both the rod and cone photoreceptor cells of the retina. The disease usually begins with damage to the rod cells, which are responsible for...
Alström Syndrome: Causes, Symptoms, Diagnosis, and Treatment in India Alström Syndrome is a rare inherited genetic disorder that affects multiple organs throughout the body, including the eyes, ears, heart, kidneys, liver, and endocrine system. One of the earliest and most noticeable features of the condition is...
Bietti’s Crystalline Dystrophy: Causes, Symptoms, Diagnosis, and Treatment Bietti’s Crystalline Dystrophy (BCD) is a rare inherited retinal disorder characterized by the accumulation of tiny yellow-white crystalline deposits in the retina and, in some cases, the cornea. Over time, these deposits are associated with progressive degeneration of...
Bardet-Biedl Syndrome: Causes, Symptoms, Diagnosis, and Treatment in India Bardet-Biedl Syndrome (BBS) is a rare inherited genetic disorder that affects multiple organs and systems in the body. It is characterized by progressive retinal degeneration, vision loss, obesity, kidney abnormalities, extra fingers or toes (polydactyly), learning difficulties,...
