Keratoconus in Costello Syndrome
Author:
Affiliation:
1. Division of Medical Genetics; A. I. duPont Hospital for Children; Wilmington, Delaware
2. Division of Clinical Genetics; Levine Children's Hospital; Charlotte, North Carolina
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.35816/fullpdf
Reference46 articles.
1. Refractive errors and strabismus in children with Laurence-Moon-Biedl syndrome;Akinci;J Pediatr Ophthalmol Strabismus,2010
2. Brittle cornea syndrome and its delineation from the kyphoscoliotic type of Ehlers-Danlos syndrome (EDS VI): Report on 23 patients and review of the literature;Al-Hussain;Am J Med Genet Part A,2004
3. Woodhouse Sakati syndrome associated with bilateral keratoconus;Al-Swailem;Brit J Ophthalmol,2006
4. Germline mutations in HRAS proto-oncogene cause Costello syndrome;Aoki;Nat Genet,2005
5. Noonan's syndrome with keratoconus and optic disc coloboma;Ascaso;Europ J Ophthalmol,1993
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1. Anterior lenticular opacities in Costello Syndrome;American Journal of Ophthalmology Case Reports;2021-06
2. Costello syndrome: Clinical phenotype, genotype, and management guidelines;American Journal of Medical Genetics Part A;2019-06-20
3. Retinal dystrophy in two boys with Costello syndrome due to the HRAS p.Gly13Cys mutation;American Journal of Medical Genetics Part A;2017-03-23
4. Treatment options for advanced keratoconus: A review;Survey of Ophthalmology;2015-09
5. Genetics of Keratoconus: Where Do We Stand?;Journal of Ophthalmology;2014
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