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Xu, C. Lattice Corneal Dystrophy Type II. Encyclopedia. Available online: https://encyclopedia.pub/entry/4467 (accessed on 29 September 2026).
Xu C. Lattice Corneal Dystrophy Type II. Encyclopedia. Available at: https://encyclopedia.pub/entry/4467. Accessed September 29, 2026.
Xu, Camila. "Lattice Corneal Dystrophy Type II" Encyclopedia, https://encyclopedia.pub/entry/4467 (accessed September 29, 2026).
Xu, C. (2020, December 23). Lattice Corneal Dystrophy Type II. In Encyclopedia. https://encyclopedia.pub/entry/4467
Xu, Camila. "Lattice Corneal Dystrophy Type II." Encyclopedia. Web. 23 December, 2020.
Lattice Corneal Dystrophy Type II
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This entry is adapted from the peer-reviewed paper https://medlineplus.gov/genetics/condition/lattice-corneal-dystrophy-type-ii

Lattice corneal dystrophy type II is characterized by an accumulation of protein clumps called amyloid deposits in tissues throughout the body.

genetic conditions

References

  1. Carrwik C, Stenevi U. Lattice corneal dystrophy, gelsolin type (Meretoja'ssyndrome). Acta Ophthalmol. 2009 Nov;87(8):813-9. doi:10.1111/j.1755-3768.2009.01686.x. Review.
  2. Klintworth GK. Corneal dystrophies. Orphanet J Rare Dis. 2009 Feb 23;4:7. doi:10.1186/1750-1172-4-7. Review.
  3. Levy E, Haltia M, Fernandez-Madrid I, Koivunen O, Ghiso J, Prelli F, FrangioneB. Mutation in gelsolin gene in Finnish hereditary amyloidosis. J Exp Med. 1990Dec 1;172(6):1865-7.
  4. Paunio T, Kangas H, Kalkkinen N, Haltia M, Palo J, Peltonen L. Towardunderstanding the pathogenic mechanisms in gelsolin-related amyloidosis: in vitroexpression reveals an abnormal gelsolin fragment. Hum Mol Genet. 1994Dec;3(12):2223-9.
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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: 714
Entry Collection: MedlinePlus
Revision: 1 time (View History)
Update Date: 23 Dec 2020
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