References
- Girelli D, Olivieri O, De Franceschi L, et al. A linkage between hereditary hyperferritinaemia not related to iron overload and autosomal dominant congenital cataract. Br J Haematol. 1995;90(4):931–934.
- Bonneau D, Winter-Fuseau I, Loiseau MN, et al. Bilateral cataract and high serum ferritin: a new dominant genetic disorder?. J Med Genet. 1995;32(10):778–779. doi: 10.1136/jmg.32.10.778.
- Millonig G, Muckenthaler MU, Mueller S. Hyperferritinaemia-cataract syndrome: worldwide mutations and phenotype of an increasingly diagnosed genetic disorder. Hum Genomics. 2010;4:250–262.
- Lindberg K, Hellebostad M. Hyperferritinaemia-cataract syndrome. Acta Ophthalmol Scand. 1999;77(4):478–480.
- Tuysuz G, Ozdemir N, Sonmez E, et al. A new family with hereditary hyperferritinemia cataract syndrome. Genet Couns. 2013;24:393–397.
- Kutlu O, Ecirli S, Sakın A, et al. Hereditary hyperferritinemia-cataract syndrome. Nobel Med. 2017;13:80–82.
- Arosio P, Ingrassia R, Cavadini P. Ferritins: a family of molecules for iron storage, antioxidation and more. Biochim Biophys Acta. 2009;1790(7):589–599. doi: 10.1016/j.bbagen.2008.09.004.
- Siddique A, Kowdley KV. Review article: the iron overload syndromes. Aliment Pharmacol Ther. 2012;35(8):876–893. doi: 10.1111/j.1365-2036.2012.05051.x.
- Yin D, Kulhalli V, Walker AP. Raised serum ferritin concentration in hereditary hyperferritinemia cataract syndrome is not a marker for iron overload. Hepatology 2014;59(3):1204–1206. doi: 10.1002/hep.26681.
- Kröger A, Bachli EB, Mumford A, et al. Hyperferritinemia without iron overload in patients with bilateral cataracts: a case series. J Med Case Rep. 2011;21:471–474.
- Brooks DG, Manova-Todorova K, Farmer J, et al. Ferritin crystal cataracts in hereditary hyperferritinemia cataract syndrome. Invest Ophthalmol Vis Sci. 2002;43(4):1121–1126.
- Bowes O, Baxter K, Elsey T, et al. Hereditary hyperferritinaemia cataract syndrome. Lancet 2014;383(9927):1520 doi: 10.1016/S0140-6736(14)60484-0.
- Platteau E, Hoornaert K, Moens K, et al. Age-dependent ocular phenotype in hereditary hyperferritinaemia cataract syndrome (HHCS). Acta Ophthalmol. 2012;90(3):e239–240. doi: 10.1111/j.1755-3768.2011.02142.x.
- Cazzola M, Bergamaschi G, Tonon L, et al. Hereditary hyperferritinemia-cataract syndrome: relationship between phenotypes and specific mutations in the iron-responsive element of ferritin light-chain mRNA. Blood 1997;90(2):814–821.