Nephropathic Cystinosis with Ocular Involvement - Two Case Reports at Campinas and Brazil

Messias PN^*, Sobrinho MVA, Hoehr GC and Selegatto LT

Department of Ophthalmology, Rua Napoleao de Barros, 1222, Brazil

*Corresponding Author : Paola Napolitano Messias
Department of Ophthalmology, Rua Napoleao de Barros, 1222, Brazil
E-mail: paola_messias@hotmail.com

Received: November 22, 2016 Accepted: February 28, 2017 Published: March 04, 2017

Citation: Messias PN, Sobrinho MVA, Hoehr GC, Selegatto LT (2017) Nephropathic Cystinosis with Ocular Involvement - Two Case Reports at Campinas and Brazil. Int J Ophthalmic Pathol 6:2. doi: 10.4172/2324-8599.1000199

Cystinosis is an autosomal recessively inherited disorder which leads to an aminoalkanoic acid crystals accumulation in tissues. In eyes, crystals accumulate within the tissue layer inflicting photophobia and eventually sightlessness, requiring anaplastic. During this research, we have a tendency to represent 2 cases, which were reported in patients with identification of Nephropathic Cystinosis and ocular manifestations, from identification through medical care and prognosis.