메뉴 건너뛰기




Volumn 47, Issue 1, 2010, Pages 29-33

High measured intraocular pressure in children with recessive congenital hereditary endothelial dystrophy

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHILD; CLINICAL ARTICLE; CONGENITAL GLAUCOMA; FEMALE; HUMAN; INFANT; INTRAOCULAR PRESSURE; MALE; OPTIC NERVE; PRESCHOOL CHILD; RETINOSCOPY; SCHOOL CHILD; SLIT LAMP; VISUAL ACUITY;

EID: 76149131704     PISSN: 01913913     EISSN: None     Source Type: Journal    
DOI: 10.3928/01913913-20100106-07     Document Type: Article
Times cited : (10)

References (21)
  • 3
    • 17344362827 scopus 로고    scopus 로고
    • Mutations in CYP1B1, the gene for cytochrome P4501B1, are the predominant cause of primary congenital glaucoma in Saudi Arabia
    • Bejjani BA, Lewis RA, Tomey KF, et al. Mutations in CYP1B1, the gene for cytochrome P4501B1, are the predominant cause of primary congenital glaucoma in Saudi Arabia. Am J Hum Genet. 1998;62:325-233.
    • (1998) Am J Hum Genet , vol.62 , pp. 325-233
    • Bejjani, B.A.1    Lewis, R.A.2    Tomey, K.F.3
  • 4
    • 0034639693 scopus 로고    scopus 로고
    • Bejjani BA, Stockton DW, Lewis RA, et al. Multiple CYP1B1 mutations and incomplete penetrance in an inbred population segregating primary congenital glaucoma suggest frequent de novo events and a dominant modifier locus. Hum Mol Genet. 2000;9:367-374. Erratum in: Hum Mol Genet. 2000;9:1141.
    • Bejjani BA, Stockton DW, Lewis RA, et al. Multiple CYP1B1 mutations and incomplete penetrance in an inbred population segregating primary congenital glaucoma suggest frequent de novo events and a dominant modifier locus. Hum Mol Genet. 2000;9:367-374. Erratum in: Hum Mol Genet. 2000;9:1141.
  • 5
    • 33846428903 scopus 로고
    • Congenital hereditary corneal dystrophy
    • Maumenee AE. Congenital hereditary corneal dystrophy. Am J Ophthalmol. 1960;50:1114-1124.
    • (1960) Am J Ophthalmol , vol.50 , pp. 1114-1124
    • Maumenee, A.E.1
  • 6
    • 0013815166 scopus 로고
    • Congenital hereditary corneal dystrophy
    • Keates RH, Cvintal T. Congenital hereditary corneal dystrophy. Am J Ophthalmol. 1965;60:892-894.
    • (1965) Am J Ophthalmol , vol.60 , pp. 892-894
    • Keates, R.H.1    Cvintal, T.2
  • 7
    • 0017807244 scopus 로고
    • Clinical differentiation of recessive congenital hereditary endothelial dystrophy and dominant hereditary endothelial dystrophy
    • Judisch GF, Maumenee IH. Clinical differentiation of recessive congenital hereditary endothelial dystrophy and dominant hereditary endothelial dystrophy. Am J Ophthalmol. 1978;85(5 Pt 1):606-612.
    • (1978) Am J Ophthalmol , vol.85 , Issue.5 PART 1 , pp. 606-612
    • Judisch, G.F.1    Maumenee, I.H.2
  • 8
    • 33846310951 scopus 로고    scopus 로고
    • Jiao X, Sultana A, Garg P, et al. Autosomal recessive corneal endothelial dystrophy (CHED2) is associated with mutations in SLC4A11. J Med Genet. 2007;44:64-68. Erratum in: J Med Genet. 2007;44:407.
    • Jiao X, Sultana A, Garg P, et al. Autosomal recessive corneal endothelial dystrophy (CHED2) is associated with mutations in SLC4A11. J Med Genet. 2007;44:64-68. Erratum in: J Med Genet. 2007;44:407.
  • 9
    • 33745544253 scopus 로고    scopus 로고
    • Mutations in sodium-borate cotransporter SLC4A11 cause recessive congenital hereditary endothelial dystrophy (CHED2)
    • Vithana EN, Morgan P, Sundaresan P, et al. Mutations in sodium-borate cotransporter SLC4A11 cause recessive congenital hereditary endothelial dystrophy (CHED2). Nat Genet. 2006;38:755-757.
    • (2006) Nat Genet , vol.38 , pp. 755-757
    • Vithana, E.N.1    Morgan, P.2    Sundaresan, P.3
  • 10
    • 0028893448 scopus 로고
    • Results of penetrating keratoplasty in CHED: Congenital hereditary endothelial dystrophy
    • Sajjadi H, Javadi MA, Hemmati R, Mirdeghan A, Parvin M, Nassiri N. Results of penetrating keratoplasty in CHED: congenital hereditary endothelial dystrophy. Cornea. 1995;14:18-25.
    • (1995) Cornea , vol.14 , pp. 18-25
    • Sajjadi, H.1    Javadi, M.A.2    Hemmati, R.3    Mirdeghan, A.4    Parvin, M.5    Nassiri, N.6
  • 11
    • 0027291601 scopus 로고
    • Sources of error with use of Goldmann-type tonometers
    • Whitacre MM, Stein R. Sources of error with use of Goldmann-type tonometers. Surv Ophthalmol. 1993;38:1-30.
    • (1993) Surv Ophthalmol , vol.38 , pp. 1-30
    • Whitacre, M.M.1    Stein, R.2
  • 12
    • 0018575310 scopus 로고
    • Increase in axial length of the macaque monkey eye after corneal opacification
    • Wiesel TN, Raviola E. Increase in axial length of the macaque monkey eye after corneal opacification. Invest Ophthalmol Vis Sci. 1979;18:1232-1236.
    • (1979) Invest Ophthalmol Vis Sci , vol.18 , pp. 1232-1236
    • Wiesel, T.N.1    Raviola, E.2
  • 13
    • 33646901276 scopus 로고    scopus 로고
    • Measuring intraocular pressure-adjustments for corneal thickness and new technologies
    • Herndon LW. Measuring intraocular pressure-adjustments for corneal thickness and new technologies. Curr Opin Ophthalmol. 2006;17:115-119.
    • (2006) Curr Opin Ophthalmol , vol.17 , pp. 115-119
    • Herndon, L.W.1
  • 15
    • 35848966791 scopus 로고    scopus 로고
    • What biomechanical properties of the cornea are relevant for the clinician?
    • Kotecha A. What biomechanical properties of the cornea are relevant for the clinician? Surv Ophthalmol. 2007;52(suppl 2):S109-S114.
    • (2007) Surv Ophthalmol , vol.52 , Issue.SUPPL. 2
    • Kotecha, A.1
  • 16
    • 39749171797 scopus 로고    scopus 로고
    • Central corneal thickness in children: Does it help or hinder our evaluation of eyes at risk for glaucoma?
    • Freedman SF. Central corneal thickness in children: does it help or hinder our evaluation of eyes at risk for glaucoma? J AAPOS. 2008;12:1-2.
    • (2008) J AAPOS , vol.12 , pp. 1-2
    • Freedman, S.F.1
  • 17
    • 0024426247 scopus 로고
    • Anterior mesenchymal dysgenesis of the eye: Congenital hereditary endothelial dystrophy and congenital glaucoma
    • Pedersen OO, Rushood A, Olsen EG. Anterior mesenchymal dysgenesis of the eye: congenital hereditary endothelial dystrophy and congenital glaucoma. Acta Ophthalmol (Copenh). 1989;67:470-476.
    • (1989) Acta Ophthalmol (Copenh) , vol.67 , pp. 470-476
    • Pedersen, O.O.1    Rushood, A.2    Olsen, E.G.3
  • 18
    • 0028838036 scopus 로고
    • Congenital hereditary endothelial dystrophy associated with glaucoma
    • Mullaney PB, Risco JM, Teichmann K, Millar L. Congenital hereditary endothelial dystrophy associated with glaucoma. Ophthalmology. 1995;102:186-192.
    • (1995) Ophthalmology , vol.102 , pp. 186-192
    • Mullaney, P.B.1    Risco, J.M.2    Teichmann, K.3    Millar, L.4
  • 20
    • 33847266341 scopus 로고    scopus 로고
    • Primary pediatric keratoplasty: Indications, graft survival, and visual outcome
    • Al-Ghamdi A, Al-Rajhi A, Wagoner MD. Primary pediatric keratoplasty: indications, graft survival, and visual outcome. J AAPOS. 2007;11:41-47.
    • (2007) J AAPOS , vol.11 , pp. 41-47
    • Al-Ghamdi, A.1    Al-Rajhi, A.2    Wagoner, M.D.3
  • 21
    • 3342986341 scopus 로고    scopus 로고
    • Outcome of combined Ahmed glaucoma valve implant and penetrating keratoplasty in refractory congenital glaucoma with corneal opacity
    • Al-Torbak AA. Outcome of combined Ahmed glaucoma valve implant and penetrating keratoplasty in refractory congenital glaucoma with corneal opacity. Cornea. 2004;23:554-559.
    • (2004) Cornea , vol.23 , pp. 554-559
    • Al-Torbak, A.A.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.