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Xu, C. Lattice Corneal Dystrophy Type I. Encyclopedia. Available online: https://encyclopedia.pub/entry/4469 (accessed on 29 September 2026).
Xu C. Lattice Corneal Dystrophy Type I. Encyclopedia. Available at: https://encyclopedia.pub/entry/4469. Accessed September 29, 2026.
Xu, Camila. "Lattice Corneal Dystrophy Type I" Encyclopedia, https://encyclopedia.pub/entry/4469 (accessed September 29, 2026).
Xu, C. (2020, December 23). Lattice Corneal Dystrophy Type I. In Encyclopedia. https://encyclopedia.pub/entry/4469
Xu, Camila. "Lattice Corneal Dystrophy Type I." Encyclopedia. Web. 23 December, 2020.
Lattice Corneal Dystrophy Type I
Edit
This entry is adapted from the peer-reviewed paper https://medlineplus.gov/genetics/condition/lattice-corneal-dystrophy-type-i

Lattice corneal dystrophy type I is an eye disorder that affects the clear, outer covering of the eye called the cornea.

genetic conditions

References

  1. Kannabiran C, Klintworth GK. TGFBI gene mutations in corneal dystrophies. Hum Mutat. 2006 Jul;27(7):615-25. Review.
  2. Klintworth GK. Corneal dystrophies. Orphanet J Rare Dis. 2009 Feb 23;4:7. doi:10.1186/1750-1172-4-7. Review.
  3. Liu Z, Wang YQ, Gong QH, Xie LX. An R124C mutation in TGFBI caused latticecorneal dystrophy type I with a variable phenotype in three Chinese families. MolVis. 2008 Jun 30;14:1234-9.
  4. Munier FL, Korvatska E, Djemaï A, Le Paslier D, Zografos L, Pescia G,Schorderet DF. Kerato-epithelin mutations in four 5q31-linked cornealdystrophies. Nat Genet. 1997 Mar;15(3):247-51.
  5. Schmitt-Bernard CF, Chavanieu A, Derancourt J, Arnaud B, Demaille JG, Calas B,Argiles A. In vitro creation of amyloid fibrils from native and Arg124Cys mutatedbetaIGH3((110-131)) peptides, and its relevance for lattice corneal amyloiddystrophy type I. Biochem Biophys Res Commun. 2000 Jul 5;273(2):649-53.
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Subjects: Genetics & Heredity
Contributor MDPI registered users' name will be linked to their SciProfiles pages. To register with us, please refer to https://encyclopedia.pub/register : Camila Xu
View Times: 726
Entry Collection: MedlinePlus
Revision: 1 time (View History)
Update Date: 23 Dec 2020
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