Letter to the Editor: Characterization of Choriocapillaris and Choroidal Abnormalities in Alport Syndrome

Author:

Bosnar Damir123,Knežić Zagorec Mira124,Bušić Mladen123,Cigić Valentina12,Zagorec Nikola5,Nikuševa Martić Tamara6,Galešić Ljubanović Danica78

Affiliation:

1. Department of Ophthalmology, Reference Center of the Ministry of Health of the Republic of Croatia for Pediatric Ophthalmology and Strabismus, University Hospital “Sveti Duh,” Zagreb, Croatia

2. Faculty of Dental Medicine and Health Osijek, Josip Juraj Strossmayer University of Osijek, Osijek, Croatia

3. Faculty of Medicine Osijek, Josip Juraj Strossmayer University of Osijek, Osijek, Croatia

4. mira.knezic94@gmail.com

5. Department of Nephrology and Dialysis, Dubrava University Hospital, Zagreb, Croatia

6. Department of Medical Biology and Genetics, School of Medicine, University of Zagreb, Zagreb, Croatia

7. Institute of Pathology, School of Medicine, University of Zagreb, Zagreb, Croatia

8. Department of Nephropatology and Electron Microscopy, Dubrava University Hospital, Zagreb, Croatia.

Publisher

Association for Research in Vision and Ophthalmology (ARVO)

Subject

Ophthalmology,Biomedical Engineering

Reference15 articles.

1. Characterization of choriocapillaris and choroidal abnormalities in Alport syndrome;Cicinelli;Transl Vis Sci Technol,2022

2. The response of retinal vasculature to angiotensin;Rockwood;Invest Ophthalmol Vis Sci,1987

3. Angiotensin II and its receptor subtypes in the human eye;Senanayake;Invest Ophthalmol Vis Sci,2003

4. Short-term effect of angiotensin converting enzyme inhibitor on choroidal vascularity;Temel;Photodiagnosis Photodyn Ther,2021

5. Early angiotensin-converting enzyme inhibition in Alport syndrome delays renal failure and improves life expectancy;Gross;Kidney Int,2012

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