Giant Macular Hole in Alport Syndrome
Author:
Publisher
Informa UK Limited
Subject
Genetics(clinical),Ophthalmology,Pediatrics, Perinatology, and Child Health
Link
http://www.tandfonline.com/doi/pdf/10.3109/13816811003767128
Reference16 articles.
1. Identification of a distinct type IV collagen alpha chain with restricted kidney distribution and assignment of its gene to the locus of X chromosome-linked Alport syndrome.
2. A review of the ocular manifestations
3. Alport's syndrome with bilateral macular hole
4. BILATERAL MACULAR HOLES: AN UNUSUAL FEATURE OF ALPORT SYNDROME
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1. Frail inner limiting membrane maculopathy suggested to describe a new retinal Alport-like condition with two variants in three generations of females;Ophthalmic Genetics;2024-01-10
2. Sealed Unilateral Full-Thickness Macular Hole with Amniotic Membrane Graft in a Patient with Alport Syndrome: A Case Report;Case Reports in Ophthalmology;2023-10-18
3. Multidisciplinary and multidimensional approaches to transplantation in children with rare genetic kidney diseases;Pediatric Transplantation;2023-07-31
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5. Okuläre Veränderungen bei Patienten mit Alport-Syndrom – ein Update;Die Ophthalmologie;2023-02-08
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