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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.

Murro, V., Mucciolo, D. P., Sodi, A., Vannozzi, L., De Libero, C., Simonini, G., Rizzo, S., Retinal capillaritis in a CRB1-associated retinal dystrophy, <<OPHTHALMIC GENETICS>>, 2017; 38 (6): 555-558. [doi:10.1080/13816810.2017.1281966] [https://hdl.handle.net/10807/247946]

Retinal capillaritis in a CRB1-associated retinal dystrophy

Murro V.;Mucciolo D. P.;Sodi A.;Vannozzi L.;De Libero C.;Simonini G.;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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	Anno pubblicazione
	
				2017
			
	Lingua del contenuto
	
				Inglese
			
	Nome del periodico
	
				OPHTHALMIC GENETICS
			
	DOI del contributo
	
				https://dx.doi.org/10.1080/13816810.2017.1281966
			
	Citazione
	
				Murro, V., Mucciolo, D. P., Sodi, A., Vannozzi, L., De Libero, C., Simonini, G., Rizzo, S., Retinal capillaritis in a CRB1-associated retinal dystrophy, <<OPHTHALMIC GENETICS>>, 2017;  38 (6): 555-558. [doi:10.1080/13816810.2017.1281966] [https://hdl.handle.net/10807/247946]
			
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/10807/247946

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