181 related articles for article (PubMed ID: 37107549)
1. The Role of Genetic Testing in Children Requiring Surgery for Ectopia Lentis.
Musleh M; Bull A; Linton E; Liu J; Waller S; Hardcastle C; Clayton-Smith J; Sharma V; Black GC; Biswas S; Ashworth JL; Sergouniotis PI
Genes (Basel); 2023 Mar; 14(4):. PubMed ID: 37107549
[TBL] [Abstract][Full Text] [Related]
2. A genotype-phenotype comparison of ADAMTSL4 and FBN1 in isolated ectopia lentis.
Chandra A; Aragon-Martin JA; Hughes K; Gati S; Reddy MA; Deshpande C; Cormack G; Child AH; Charteris DG; Arno G
Invest Ophthalmol Vis Sci; 2012 Jul; 53(8):4889-96. PubMed ID: 22736615
[TBL] [Abstract][Full Text] [Related]
3. A novel ADAMTSL4 compound heterozygous mutation in isolated ectopia lentis: a case report and review of the literature.
Wei H; Meng X; Qin H; Li X
J Med Case Rep; 2023 Dec; 17(1):532. PubMed ID: 38146062
[TBL] [Abstract][Full Text] [Related]
4. Risk factors for postoperative complications in lensectomy-vitrectomy with or without intraocular lens placement in ectopia lentis associated with Marfan syndrome.
Fan F; Luo Y; Liu X; Lu Y; Zheng T
Br J Ophthalmol; 2014 Oct; 98(10):1338-42. PubMed ID: 24831716
[TBL] [Abstract][Full Text] [Related]
5. Early onset ectopia lentis due to a FBN1 mutation with non-penetrance.
Zhang L; Lai YH; Capasso JE; Han S; Levin AV
Am J Med Genet A; 2015 Jun; 167(6):1365-8. PubMed ID: 25900864
[TBL] [Abstract][Full Text] [Related]
6. [Hereditary ectopia lentis: diagnosis and surgical treatment].
Chizhonkova EA; Avetisov KS; Avetisov SE
Vestn Oftalmol; 2023; 139(1):129-136. PubMed ID: 36924525
[TBL] [Abstract][Full Text] [Related]
7. Ectopia lentis as the presenting and primary feature in Marfan syndrome.
Zadeh N; Bernstein JA; Niemi AK; Dugan S; Kwan A; Liang D; Hyland JC; Hoyme HE; Hudgins L; Manning MA
Am J Med Genet A; 2011 Nov; 155A(11):2661-8. PubMed ID: 21932315
[TBL] [Abstract][Full Text] [Related]
8. Confirmation of ADAMTSL4 mutations for autosomal recessive isolated bilateral ectopia lentis.
Greene VB; Stoetzel C; Pelletier V; Perdomo-Trujillo Y; Liebermann L; Marion V; De Korvin H; Boileau C; Dufier JL; Dollfus H
Ophthalmic Genet; 2010 Mar; 31(1):47-51. PubMed ID: 20141359
[TBL] [Abstract][Full Text] [Related]
9. A FBN1 mutation association with different phenotypes of Marfan syndrome in a Chinese family.
Li Y; Xu J; Chen M; Du B; Li Q; Xing Q; Zhang Y
Clin Chim Acta; 2016 Sep; 460():102-6. PubMed ID: 27353645
[TBL] [Abstract][Full Text] [Related]
10. Combination of Panel-based Next-Generation Sequencing and Clinical Findings in Congenital Ectopia Lentis Diagnosed in Chinese Patients.
Chen TH; Chen ZX; Zhang M; Chen JH; Deng M; Zheng JL; Lan LN; Jiang YX
Am J Ophthalmol; 2022 May; 237():278-289. PubMed ID: 34818515
[TBL] [Abstract][Full Text] [Related]
11. Congenital megalocornea with zonular weakness and childhood lens-related secondary glaucoma - a distinct phenotype caused by recessive LTBP2 mutations.
Khan AO; Aldahmesh MA; Alkuraya FS
Mol Vis; 2011; 17():2570-9. PubMed ID: 22025892
[TBL] [Abstract][Full Text] [Related]
12. Axial growth and binocular function following bilateral lensectomy and scleral fixation of an intraocular lens in nontraumatic ectopia lentis.
Park SC; Chung ES; Chung TY; Kim SA; Oh SY
Jpn J Ophthalmol; 2010 May; 54(3):232-8. PubMed ID: 20577858
[TBL] [Abstract][Full Text] [Related]
13. Bimanual irrigation-aspiration for ectopia lentis and use of a small incision for 4-point scleral-sutured foldable intraocular lens and anterior vitrectomy in patients with Marfan syndrome.
Wang Z; Lu Y; Xiao K; Gao Y; He J; Zhang S; Wang G; Zhang M
Indian J Ophthalmol; 2019 Oct; 67(10):1629-1633. PubMed ID: 31546497
[TBL] [Abstract][Full Text] [Related]
14. A cohort study of multiple families with FBN1 p.R650C variant, ectopia lentis, and low but not absent risk for aortopathy.
Vatti L; Fitzgerald-Butt SM; McBride KL
Am J Med Genet A; 2017 Nov; 173(11):2995-3002. PubMed ID: 28941062
[TBL] [Abstract][Full Text] [Related]
15. Iris-claw intraocular lens implantation in children with ectopia lentis.
Çevik SG; Çevik MÖ; Özmen AT
Arq Bras Oftalmol; 2017; 80(2):114-117. PubMed ID: 28591285
[TBL] [Abstract][Full Text] [Related]
16. Ectopia lentis surgery in Marfan's syndrome: from "couching" to the use of intracapsular tension rings.
Dogăroiu AC; Dogăroiu C; Tătaru CP
Rom J Ophthalmol; 2022; 66(1):2-7. PubMed ID: 35531445
[TBL] [Abstract][Full Text] [Related]
17. Genotype variant screening and phenotypic analysis of
Zhou Y; Guo D; Cao Q; Zhang X; Jin G; Zheng D
Mol Med Rep; 2021 Apr; 23(4):. PubMed ID: 33576469
[TBL] [Abstract][Full Text] [Related]
18. Novel p.G1344E mutation in
Yang Y; Zhou YL; Yao TT; Pan H; Gu P; Wang ZY
Br J Ophthalmol; 2021 Mar; 105(3):341-347. PubMed ID: 32404357
[TBL] [Abstract][Full Text] [Related]
19. Clinical and genetic findings in Chinese families with congenital ectopia lentis.
Liu X; Niu L; Zhang L; Jiang L; Liu K; Wu X; Liu X; Wang J
Mol Genet Genomic Med; 2023 May; 11(5):e2140. PubMed ID: 36670079
[TBL] [Abstract][Full Text] [Related]
20. The phenotypic spectrum of
Knight LSW; Mullany S; Taranath DA; Ruddle JB; Barnett CP; Sallevelt SCEH; Berry EC; Marshall HN; Hollitt GL; Souzeau E; Craig JE; Siggs OM
Mol Vis; 2022; 28():257-268. PubMed ID: 36284667
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
