Cerebroretinal microangiopathy with calcifications and cysts 2
MONDO:0015026Any Coats plus syndrome in which the cause of the disease is a mutation in the STN1 gene.
Also known as: Coats plus syndrome caused by mutation in STN1, STN1 Coats plus syndrome, cerebroretinal microangiopathy with calcifications and cysts 2, cerebroretinal microangiopathy with calcifications and cysts type 2, CRMCC2
24 clinical trials for this condition and its sub-types.
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Experimental infusion aims to fix bone marrow failure in rare telomere disease
Disease control OngoingThis early-stage trial tests a single infusion of EXG34217 in 12 people aged 12 and older who have bone marrow failure due to telomere biology disorders. The main goal is to check safety and tolerability, while also looking at changes in telomere length and blood cell counts. Bec…
Phase: PHASE1 • Sponsor: Elixirgen Therapeutics, Inc. • Aim: Disease control
Last updated Jun 27, 2026 09:02 UTC
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Free eye tests aim to catch vision loss early in harlem and washington heights
Knowledge-focused OngoingThis study offers free vision screenings to underserved adults over 40 living in affordable housing in Harlem and Washington Heights. The goal is to find eye problems like glaucoma, cataracts, and diabetic retinopathy early and connect people with follow-up care. About 749 partic…
Phase: NA • Sponsor: Columbia University • Aim: Knowledge-focused
Last updated Jun 27, 2026 07:54 UTC