Posterior amorphous corneal dystrophy in a patient with 12q21.33 deletion-Reference-Cited by-同舟云学术

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Posterior amorphous corneal dystrophy in a patient with 12q21.33 deletion

Published:2018-07-30 Issue:5 Volume:39 Page:645-647
ISSN:1381-6810
Container-title:Ophthalmic Genetics
language:en
Short-container-title:Ophthalmic Genetics

Author:

Lenk Janine¹,Porrmann Joseph²,Smitka Martin³,Eger Ines⁴,Schröck Evelin²,Hackmann Karl²,Herber Robert¹,Raiskup Frederik¹,Tzschach Andreas²^ORCID

Affiliation:

1. Department of Ophthalmology, Universitätsklinikum Carl Gustav Carus, Dresden, Germany

2. Institut für Klinische Genetik, Technische Universität Dresden, Dresden, Germany

3. Children’s hospital, Universitätsklinikum Carl Gustav Carus, Dresden, Germany

4. Children’s hospital, Städtisches Klinikum Görlitz, Görlitz, Germany

Publisher

Informa UK Limited

Subject

Genetics (clinical),Ophthalmology,Pediatrics, Perinatology and Child Health

Link

https://www.tandfonline.com/doi/pdf/10.1080/13816810.2018.1502792

Reference13 articles.

1. Posterior Amorphous Corneal Dystrophy Associated With Keratoglobus: A Case Report

2. New Findings in Posterior Amorphous Corneal Dystrophy

3. The Pathology of Posterior Amorphous Corneal Dystrophy

4. Posterior Amorphous Corneal Dystrophy Is Associated with a Deletion of Small Leucine-rich Proteoglycans on Chromosome 12

5. Linkage of Posterior Amorphous Corneal Dystrophy to Chromosome 12q21.33 and Exclusion of Coding Region Mutations inKERA,LUM,DCN, andEPYC

Cited by 6 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Cornea and Sclera;Ocular Pathology;2025

2. Petal-shaped corneal pattern in a patient with posterior amorphous corneal dystrophy;American Journal of Ophthalmology Case Reports;2024-09

3. Expanding the phenotype of 12q21 deletions: A role of BTG1 in speech development?;European Journal of Medical Genetics;2023-04

4. 12q21 Interstitial Deletions: Seven New Syndromic Cases Detected by Array-CGH and Review of the Literature;Genes;2022-04-27

5. Posterior Amorphous Corneal Dystrophy: New Chromosomal Breakpoints in the Small Leucine-Rich Proteoglycan-Coding Region;Cornea;2022-01-17

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