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Results 1 - 10 of 21 for Central corneal dystrophy
  1. Meesmann corneal dystrophy 
    ... Citation on PubMed or Free article on PubMed Central
    https://medlineplus.gov/.../condition/meesmann-corneal-dystrophy - Genetics
  2. Congenital stromal corneal dystrophy 
    ... Citation on PubMed or Free article on PubMed Central Rodahl E, Knappskog PM, Bredrup C, Boman H. Congenital Stromal Corneal Dystrophy. 2008 Nov 25 [updated 2018 Nov 29]. In: ...
    https://medlineplus.gov/.../congenital-stromal-corneal-dystrophy - Genetics
  3. Lattice corneal dystrophy type I 
    ... Citation on PubMed or Free article on PubMed Central Liu Z, Wang YQ, Gong QH, Xie LX. An R124C mutation in TGFBI caused lattice corneal dystrophy type I with a variable phenotype in three ...
    https://medlineplus.gov/.../lattice-corneal-dystrophy-type-i - Genetics
  4. Fuchs endothelial dystrophy 
    ... Citation on PubMed or Free article on PubMed Central Afshari NA, Li YJ, Pericak-Vance MA, Gregory S, Klintworth GK. Genome-wide linkage scan in fuchs endothelial corneal dystrophy. Invest Ophthalmol Vis Sci. 2009 Mar;50(3): ...
    https://medlineplus.gov/.../condition/fuchs-endothelial-dystrophy - Genetics
  5. Lattice corneal dystrophy type II 
    ... Citation on PubMed or Free article on PubMed Central Paunio T, Kangas H, Kalkkinen N, ... Citation on PubMed
    https://medlineplus.gov/.../lattice-corneal-dystrophy-type-ii - Genetics
  6. COL8A2 gene 
    ... Citation on PubMed or Free article on PubMed Central Gottsch ... subtype of fuchs corneal dystrophy. Invest Ophthalmol Vis Sci. 2005 Jun;46(6): ...
    https://medlineplus.gov/genetics/gene/col8a2 - Genetics
  7. Patient support and advocacy groups 
    ... Foundation Chromosome 18 Registry & Research Society Chromosome 22 Central ... Foundation Cornelia de Lange Syndrome Foundation Costello Kids ...
    https://medlineplus.gov/about/general/genetics/supportadvocacygroups -
  8. TGFBI gene 
    ... of TGFBI gene mutations in Chinese patients with corneal dystrophies and review of the literature. Mol Vis. 2010 Jun 30;16:1186-93. Citation on PubMed or Free article on PubMed Central
    https://medlineplus.gov/genetics/gene/tgfbi - Genetics
  9. KRT12 gene 
    ... gene and detection of four mutations in Meesmann corneal epithelial dystrophy. Am J Hum Genet. 1997 Dec;61(6):1268-75. doi: 10.1086/301650. Citation on PubMed or Free article on PubMed Central
    https://medlineplus.gov/genetics/gene/krt12 - Genetics
  10. KRT3 gene 
    ... M, Ploski R, Szaflik J. Genetics of Meesmann corneal dystrophy: a novel mutation in the keratin 3 gene in an asymptomatic family suggests genotype-phenotype correlation. Mol Vis. 2008 Sep 15;14:1713-8. Citation on PubMed or Free article on PubMed Central
    https://medlineplus.gov/genetics/gene/krt3 - Genetics
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