Teaching NeuroImages: Adult-onset leukoencephalopathy with intracranial calcifications and cysts (Labrune syndrome)
تويتر \ M. Taimur Shujaat على تويتر: "Labrune syndrome (LCC) = Leukoencephalopathy with Calcifications (basal/cerebellar GM, central WM) & Cysts (edematous, can enlarge and compress +/- wall enhancement). Age: Infants to young
![Cerebro-retinal microangiopathy with calcifications and cysts due to recessive mutations in the CTC1 gene - ScienceDirect Cerebro-retinal microangiopathy with calcifications and cysts due to recessive mutations in the CTC1 gene - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0035378715006542-gr1.jpg)
Cerebro-retinal microangiopathy with calcifications and cysts due to recessive mutations in the CTC1 gene - ScienceDirect
![PDF) Retinopathy and bone marrow failure revealing Coats plus syndrome | Paula Kjöllerström - Academia.edu PDF) Retinopathy and bone marrow failure revealing Coats plus syndrome | Paula Kjöllerström - Academia.edu](https://0.academia-photos.com/attachment_thumbnails/73665654/mini_magick20211026-25666-1ahrl6n.png?1635258398)
PDF) Retinopathy and bone marrow failure revealing Coats plus syndrome | Paula Kjöllerström - Academia.edu
![Novel compound heterozygous STN1 variants are associated with Coats Plus syndrome - Acharya - 2021 - Molecular Genetics & Genomic Medicine - Wiley Online Library Novel compound heterozygous STN1 variants are associated with Coats Plus syndrome - Acharya - 2021 - Molecular Genetics & Genomic Medicine - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/4b93913d-6b5c-4590-8cae-3b824b9e1913/mgg31708-fig-0001-m.jpg)
Novel compound heterozygous STN1 variants are associated with Coats Plus syndrome - Acharya - 2021 - Molecular Genetics & Genomic Medicine - Wiley Online Library
![PDF] Mutations in STN1 cause Coats plus syndrome and are associated with genomic and telomere defects | Semantic Scholar PDF] Mutations in STN1 cause Coats plus syndrome and are associated with genomic and telomere defects | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/907bce1bf580cae0aeeede165c065630280da1ab/3-Figure1-1.png)
PDF] Mutations in STN1 cause Coats plus syndrome and are associated with genomic and telomere defects | Semantic Scholar
![Coats plus syndrome phenotype and mutation analysis of the CTC1 and... | Download Scientific Diagram Coats plus syndrome phenotype and mutation analysis of the CTC1 and... | Download Scientific Diagram](https://www.researchgate.net/profile/Arun-Kumar-257/publication/272364410/figure/fig1/AS:271488909574164@1441739408965/Coats-plus-syndrome-phenotype-and-mutation-analysis-of-the-CTC1-and-HES7-in-the-family.png)
Coats plus syndrome phenotype and mutation analysis of the CTC1 and... | Download Scientific Diagram
![Coats plus syndrome (cerebroretinal microangiopathy with calcifications and cysts‐1): A case report - Morgado - 2021 - Pediatric Dermatology - Wiley Online Library Coats plus syndrome (cerebroretinal microangiopathy with calcifications and cysts‐1): A case report - Morgado - 2021 - Pediatric Dermatology - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/bd2d04ea-052a-4f18-9a1a-d30e96f195bf/pde14366-fig-0001-m.jpg)