Fabry disease (FD) is a X-linked recessive lysosomal storage disorder characterized by altered biodegradation of glycosphingolipids. It is a multisystem pathology, also involving ophthalmological systems that show modifications of the vessel wall due to glycosphingolipid deposits. Optical coherence tomography angiography (OCT-A) allows for an objective analysis of retinal microvasculature alterations, evaluating retinal vessel density in macular region.

Optical Coherence Tomography Angiography Findings in Fabry Disease / Cennamo, Gilda; DI MAIO, LAURA GIOVANNA; Montorio, Daniela; Tranfa, Fausto; Russo, Camilla; Pontillo, Giuseppe; Cocozza, Sirio; Esposito, Roberta; DI RISI, Teodolinda; Imbriaco, Massimo; Spinelli, Letizia; Riccio, Eleonora; Pisani, Antonio. - In: JOURNAL OF CLINICAL MEDICINE. - ISSN 2077-0383. - 8:4(2019), p. 528. [10.3390/jcm8040528]

Optical Coherence Tomography Angiography Findings in Fabry Disease

Cennamo, Gilda
;
DI MAIO, LAURA GIOVANNA;Montorio, Daniela;Tranfa, Fausto;Pontillo, Giuseppe;Cocozza, Sirio;Esposito, Roberta;DI RISI, TEODOLINDA;Imbriaco, Massimo;Spinelli, Letizia;Riccio, Eleonora;Pisani, Antonio
2019

Abstract

Fabry disease (FD) is a X-linked recessive lysosomal storage disorder characterized by altered biodegradation of glycosphingolipids. It is a multisystem pathology, also involving ophthalmological systems that show modifications of the vessel wall due to glycosphingolipid deposits. Optical coherence tomography angiography (OCT-A) allows for an objective analysis of retinal microvasculature alterations, evaluating retinal vessel density in macular region.
2019
Optical Coherence Tomography Angiography Findings in Fabry Disease / Cennamo, Gilda; DI MAIO, LAURA GIOVANNA; Montorio, Daniela; Tranfa, Fausto; Russo, Camilla; Pontillo, Giuseppe; Cocozza, Sirio; Esposito, Roberta; DI RISI, Teodolinda; Imbriaco, Massimo; Spinelli, Letizia; Riccio, Eleonora; Pisani, Antonio. - In: JOURNAL OF CLINICAL MEDICINE. - ISSN 2077-0383. - 8:4(2019), p. 528. [10.3390/jcm8040528]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11588/757939
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