USANew treatments and approvals
Revakinagene taroretcel, an implanted cell therapy for MacTel type 2, approved
The FDA has approved revakinagene taroretcel for macular telangiectasia type 2.
Eye and hearing diseases
An eye disease that affects the center of the retina and gradually reduces reading vision.
Not part of the panel of Türkiye's National Newborn Screening Programme (heel-prick test). Source
This page is translated from the Turkish original.
This disease is followed through the “Eye and hearing diseases” group.
Macular telangiectasia type 2 affects an area of the eye called the macula. The macula is the center of the retina and makes detailed vision, such as reading, possible. In this disease, the very fine blood vessels in the macula become damaged and widened. It usually affects both eyes, but not always to the same degree.
The disease often appears in middle age. In the early stage there may be no symptoms. Central vision may slowly decrease over the years. Side vision is not affected; it usually does not lead to complete blindness.
The diagnosis is made with an eye examination; the pupil is widened with eye drops. Imaging that shows the layers of the retina (OCT) and images of the blood vessels are used. A simple line test called the Amsler grid may also be done.
A capsule that is placed in the eye and releases medicine to protect the retina has been developed. If new blood vessels form, injection treatments into the eye can be used. In some cases, laser treatment or surgery may be needed. The doctor who follows the disease decides which treatment is suitable.
In most people, there is no known cause. In some families, the disease occurs in more than one person. This suggests that there may be a genetic tendency; but this is not yet fully understood.
Source: American Academy of Ophthalmology – What Is Macular Telangiectasia? · EyeWiki (American Academy of Ophthalmology) – Macular telangiectasia
These facts are taken from Orphanet and MedlinePlus records (last checked: October 7, 2026). Frequency values are approximate ranges.
Non-profit patient and family organizations in Türkiye working on this disease or disease group. Links are for information; Doktorclub is not affiliated with these organizations and does not endorse them.
We could not find a patient association specific to this disease.
For all rare diseases: Nadir Hastalıklar Federasyonu
Doktorclub does not diagnose, recommend treatments or refer you to hospitals or doctors. These pages are meant to help you talk with your doctor.
USANew treatments and approvals
The FDA has approved revakinagene taroretcel for macular telangiectasia type 2.
A clinical trial is a regulated study that tests whether a new treatment is safe and whether it works, in patients who volunteer. Most trials look for a certain age, genetic change and health condition. Taking part is voluntary.
Questions you can ask your doctor
ClinicalTrials.gov lists 3 active interventional studies for this disease. 1 is recruiting now; none has a site in Türkiye. Last checked: October 7, 2026.
Selected records (studies with a site in Türkiye first):
Late stage: the effect is being compared in a large group · Phase 3 · investigational (experimental)Not yet recruitingNCT07342439
Late stage: the effect is being compared in a large group · Phase 3 · investigational (experimental)Active, not recruitingNCT06397131
Phase 4 · follow-up study of an approved drugRecruitingNCT06971939
See all studies on ClinicalTrials.gov · Joining clinical trials
TürkiyeSGK and reimbursement
A drug used for a rare disease affecting the optic nerve has been added to reimbursement coverage.
USAResearch and clinical trials
A two-year, placebo-controlled study was carried out at 7 centers in the USA.
TürkiyeResearch and clinical trials
Gazi University studied the eyes of 27 children.
These codes identify the disease in international classifications and databases. They can help when you talk with your doctor or look for reliable sources.
International rare disease database: Orphanet · ICD-11 9B75.3
Codes checked against WHO ICD-11 and Orphanet on October 6, 2026.
This page provides general information and does not replace diagnosis or treatment. Talk to your doctor about symptoms, diagnosis and treatment.