Frail inner limiting membrane maculopathy suggested to describe a new retinal Alport-like condition with two variants in three generations of females-Reference-Cited by-同舟云学术

Frail inner limiting membrane maculopathy suggested to describe a new retinal Alport-like condition with two variants in three generations of females

Published:2024-01-10 Issue:3 Volume:45 Page:281-288
ISSN:1381-6810
Container-title:Ophthalmic Genetics
language:en
Short-container-title:Ophthalmic Genetics

Author:

Petersen Sekita Dalsgård¹²^ORCID,Belmouhand Mohamed¹²,Hertz Jens Michael³⁴,Fagerberg Christina³⁴,Brasch-Andersen Charlotte³⁴,Grauslund Jakob³⁵⁶,Munier Francis L.⁷^ORCID,Larsen Michael¹²

Affiliation:

1. Faculty of Health and Medicine, University of Copenhagen, Copenhagen, Denmark

2. Department of Ophthalmology, Rigshospitalet, Copenhagen, Denmark

3. Department of Clinical Research, Faculty of Health Science, University of Southern Denmark, Odense, Denmark

4. Department of Clinical Genetics, Odense University Hospital, Odense, Denmark

5. Department of Ophthalmology, Vestfold University Trust, Tønsberg, Norway

6. Department of Ophthalmology, Odense University Hospital, Odense, Denmark

7. Jules-Gonin Eye Hospital, Fondation Asile des Aveugles, University of Lausanne, Lausanne, Switzerland

Funder

Forskningspuljen mellem Rigshospitalet og Odense Universitetshospital

Publisher

Informa UK Limited

Link

https://www.tandfonline.com/doi/pdf/10.1080/13816810.2023.2294844

Reference38 articles.

1. Challenge in pathologic diagnosis of Alport syndrome: evidence from correction of previous misdiagnosis

2. Ocular Features in Alport Syndrome: Pathogenesis and Clinical Significance

3. HEREDITARY FAMILIAL CONGENITAL HAEMORRHAGIC NEPHRITIS

4. A review of clinical characteristics and genetic backgrounds in Alport syndrome

5. Novel mutations in patients with X-linked Alport syndrome