First reported case of Doyne honeycomb retinal dystrophy (Malattia Leventinese/autosomal dominant drusen) in Scandinavia
Abstract Background Doyne honeycomb retinal dystrophy (DHRD)/malattia leventinese (ML) is an autosomal dominant, progressive retinal disorder characterized by massive central retinal drusen often partly coalescent forming a characteristic honeycomb‐like pattern. Debut of vision loss often occurs in...
Main Authors: | Inger Norlyk Sheyanth, Ihab Bishara Lolas, Henrik Okkels, Ligor Pradeep Kiruparajan, Søren Kromann Abildgaard, Michael Bjørn Petersen |
---|---|
Format: | Article |
Language: | English |
Published: |
Wiley
2021-04-01
|
Series: | Molecular Genetics & Genomic Medicine |
Subjects: | |
Online Access: | https://doi.org/10.1002/mgg3.1652 |
Similar Items
-
Long-Term Structural and Functional Assessment of Doyne Honeycomb Retinal Dystrophy following Nanosecond 2RT Laser Treatment: A Case Series
by: Andrea Cusumano, et al.
Published: (2023-11-01) -
Critica ed etica dei racconti autobiografici di malattia
by: Mariarosa Loddo
Published: (2018-12-01) -
Giustizia sociale, discriminazione sociale e malattia mentale: una ricerca attorno al mondo
by: Dinesh Bhugra
Published: (2019-09-01) -
Reconceptualizing Incarceration
by: Roberta Pandolfino
Published: (2022-09-01) -
Replication study identified EFEMP1 association with varicose vein predisposition among Indians
by: Rohit Mehra, et al.
Published: (2024-04-01)