Purpose: To report a case of CRB1-associated retinal dystrophy characterized by vitritis, retinal capillaritis, and cystoid macular edema (CME). Methods: A case report. Results: An 8-year-old boy was diagnosed with intermediate uveitis and treated with corticosteroids. He was subsequently diagnosed with retinal dystrophy and found to have two CRB1 mutations. Conclusions: Retinal capillaritis, vitritis, and CME could be inflammatory features of CRB1 retinal dystrophy in our young patient.
Retinal capillaritis in a CRB1-associated retinal dystrophy / Murro, V., Mucciolo, D.P., Sodi, A., Vannozzi, L., De Libero, C., Simonini, G., Rizzo, S.. - In: OPHTHALMIC GENETICS. - ISSN 1381-6810. - STAMPA. - 38:(2017), pp. 555-558. [10.1080/13816810.2017.1281966]
Retinal capillaritis in a CRB1-associated retinal dystrophy
Murro, Vittoria;Mucciolo, Dario Pasquale;Sodi, Andrea;Vannozzi, Lorenzo;Simonini, Gabriele;Rizzo, Stanislao
2017
Abstract
Purpose: To report a case of CRB1-associated retinal dystrophy characterized by vitritis, retinal capillaritis, and cystoid macular edema (CME). Methods: A case report. Results: An 8-year-old boy was diagnosed with intermediate uveitis and treated with corticosteroids. He was subsequently diagnosed with retinal dystrophy and found to have two CRB1 mutations. Conclusions: Retinal capillaritis, vitritis, and CME could be inflammatory features of CRB1 retinal dystrophy in our young patient.
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