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Results 1 - 10 of 12 for Macular "dystrophy," "retinal," 3
  1. ... sufficient to cause the disorder. Juvenile macular degeneration Macular dystrophy with ... National Organization for Rare Disorders (NORD) ...
  2. ... Fitzke F, et al. Mutations in the human retinal degeneration slow (RDS) gene can cause either retinitis pigmentosa or macular dystrophy. Nat Genet. 1993 Mar;3(3):213-8. doi: 10.1038/ng0393-213. ...
  3. ... Fitzke F, et al. Mutations in the human retinal degeneration slow (RDS) gene can cause either retinitis pigmentosa or macular dystrophy. Nat Genet. 1993 Mar;3(3):213-8. doi: 10.1038/ng0393-213. ...
  4. ... MICROPHTHALMIA, ISOLATED 1; MCOP1 OPTIC DISC ANOMALIES WITH RETINAL AND/OR MACULAR ... 3; MCOPCB3 MICROPHTHALMIA, ISOLATED 6; MCOP6 MICROPHTHALMIA, ISOLATED 8; ...
  5. ... Best macular dystrophy. Nat Genet. 1998 Jul;19(3):241-7. doi: 10.1038/915. ... in adult vitelliform macular dystrophy. Retina. 2004 Dec;24(6):929-39. doi: 10. ...
  6. ... K, Elliott MH, Anderson RE. Role of Stargardt-3 macular dystrophy protein (ELOVL4) in the biosynthesis of very long ... GA. Natural history of phenotypic changes in Stargardt macular dystrophy. Ophthalmic Genet. 2009 Jun;30(2):63-8. doi: 10.1080/13816810802695550. Citation on PubMed
  7. ... 2; ARMD2 MACULAR DEGENERATION, AGE-RELATED, 1; ARMD1 MACULAR DEGENERATION, AGE-RELATED, 3; ARMD3 MACULAR DEGENERATION, AGE-RELATED, 7; ARMD7 MACULAR DEGENERATION, AGE-RELATED, ...
  8. ... rod dystrophy (described above), cone dystrophy, and atrophic macular degeneration. These retinal disorders are characterized by progressive vision abnormalities, although ...
  9. ... polymorphism, complement activators, and risk of age-related macular degeneration. JAMA. 2006 Jul 19;296(3):301-9. doi: 10.1001/jama.296.3. ... role of complement Factor H in age-related macular degeneration: a review. Surv Ophthalmol. 2010 May-Jun;55(3):227-46. doi: 10.1016/j.survophthal.2009. ...
  10. ... as breakdown of the central region of the retina known as the macula (macular degeneration) with loss of specialized light receptor cells called ... p.Tyr175Phe). J Appl Genet. 2015 Aug;56(3):317-27. doi: 10.1007/s13353-015-0281-x. Epub 2015 Mar 28. Citation on PubMed or Free article on PubMed Central
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