메뉴 건너뛰기




Volumn 23, Issue 5, 2012, Pages 344-354

A new approach to the classification of neonatal corneal opacities

Author keywords

classification; corneal opacification; neonatal; Peters anomaly; sclerocornea

Indexed keywords

BACTERIAL INFECTION; BRAIN DEVELOPMENT; CLINICAL FEATURE; CORNEA DISEASE; CORNEA OPACITY; DISEASE CLASSIFICATION; EYE INJURY; GENOTYPE PHENOTYPE CORRELATION; HUMAN; KERATOPLASTY; MEDICAL TERMINOLOGY; METABOLIC DISORDER; NEONATAL CORNEA OPACITY; PETERS ANOMALY; PRIORITY JOURNAL; PROGNOSIS; REVIEW; SCLEROCORNEA; TREATMENT INDICATION; TREATMENT OUTCOME; VIRUS INFECTION; VISUAL ACUITY; VISUAL DISORDER;

EID: 84865499191     PISSN: 10408738     EISSN: 15317021     Source Type: Journal    
DOI: 10.1097/ICU.0b013e328356893d     Document Type: Review
Times cited : (46)

References (54)
  • 1
    • 0036147021 scopus 로고    scopus 로고
    • Clinicopathological correlation of congenital corneal opacification using ultrasound biomicroscopy
    • DOI 10.1136/bjo.86.1.62
    • Nischal KK, Naor J, Jay V, et al. Clinicopathological correlation of congenital corneal opacification using ultrasound biomicroscopy. Br J Ophthalmol 2002; 86:62-69. (Pubitemid 34074887)
    • (2002) British Journal of Ophthalmology , vol.86 , Issue.1 , pp. 62-69
    • Nischal, K.K.1    Naor, J.2    Jay, V.3    MacKeen, L.D.4    Rootman, D.S.5
  • 2
    • 79960006207 scopus 로고    scopus 로고
    • Chromosome abnormalities and the genetics of congenital corneal opacification
    • Mataftsi A, Islam L, Kelberman D, et al. Chromosome abnormalities and the genetics of congenital corneal opacification. Mol Vis 2011; 17:1624-1640.
    • (2011) Mol Vis , vol.17 , pp. 1624-1640
    • Mataftsi, A.1    Islam, L.2    Kelberman, D.3
  • 3
    • 35148825026 scopus 로고    scopus 로고
    • Congenital corneal opacities - A surgical approach to nomenclature and classification
    • DOI 10.1038/sj.eye.6702840, PII 6702840
    • Nischal KK. Congenital corneal opacities: a surgical approach to nomenclature and classification. Eye 2007; 21:1326-1337. (Pubitemid 47534746)
    • (2007) Eye , vol.21 , Issue.10 , pp. 1326-1337
    • Nischal, K.K.1
  • 4
    • 0032539587 scopus 로고    scopus 로고
    • Congenital eye malformations: Clinical-epidemiological analysis of 1,124,654 consecutive births in Spain
    • DOI 10.1002/(SICI)1096-8628(19980 217)75:5<497::AID-AJMG8>3. 0.CO;2-K
    • Bermejo E, Martinez-Frias ML. Congenital eye malformations: clinical epidemiological analysis of 1 124 654 consecutive births in Spain. Am J Med Genet 1998; 75:497-504. (Pubitemid 28078521)
    • (1998) American Journal of Medical Genetics , vol.75 , Issue.5 , pp. 497-504
    • Bermejo, E.1    Martinez-Frias, M.-L.2
  • 6
    • 0028895206 scopus 로고
    • Linkage of congenital hereditary endothelial dystrophy to chromosome 20
    • Toma NMG, Ebenezer ND, Inglehearn CF, et al. Linkage of congenital hereditary endothelial dystrophy to chromosome 20. Hum Mol Genet 1995; 4:2395-2398.
    • (1995) Hum Mol Genet , vol.4 , pp. 2395-2398
    • Nmg, T.1    Ebenezer, N.D.2    Inglehearn, C.F.3
  • 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; 85:606-612. (Pubitemid 8323904)
    • (1978) American Journal of Ophthalmology , vol.85 , Issue.5 , pp. 606-612
    • Judisch, G.F.1    Maumenee, I.H.2
  • 8
    • 2642649523 scopus 로고    scopus 로고
    • A morphological and functional study of congenital hereditary endothelial dystrophy
    • Ehlers N, Modis L, Moller-Pedersen T. A morphological and functional study of congenital hereditary endothelial dystrophy. Acta Ophthalmol Scand 1998; 76:314-318. (Pubitemid 28327587)
    • (1998) Acta Ophthalmologica Scandinavica , vol.76 , Issue.3 , pp. 314-318
    • Ehlers, N.1    Mdis, L.2    Moller-Pedersen, T.3
  • 9
    • 65349167054 scopus 로고    scopus 로고
    • The IC3D classification of the corneal dystrophies
    • Weiss JS, Møller HU, Lisch W, et al. The IC3D classification of the corneal dystrophies. Cornea 2008; 27 (Suppl 2):S1-S83.
    • (2008) Cornea , vol.27 , Issue.SUPPL. 2
    • Weiss, J.S.1    Møller, H.U.2    Lisch, W.3
  • 10
    • 81355127411 scopus 로고    scopus 로고
    • A novel mutation of the decorin gene identified in a Korean family with congenital hereditary stromal dystrophy
    • Kim JH, Ko JM, Lee I, et al. A novel mutation of the decorin gene identified in a Korean family with congenital hereditary stromal dystrophy. Cornea 2011; 30:1473-1477.
    • (2011) Cornea , vol.30 , pp. 1473-1477
    • Kim, J.H.1    Ko, J.M.2    Lee, I.3
  • 11
    • 34447517518 scopus 로고    scopus 로고
    • Coexistent congenital hereditary endothelial dystrophy and congenital glaucoma
    • DOI 10.1097/ICO.0b013e31804e4579, PII 0000322620070700000001
    • Ramamurthy B, Sachdeva V, Mandal AK, et al. Coexistent congenital hereditary endothelial dystrophy and congenital glaucoma. Cornea 2007; 26:647-649. (Pubitemid 47080279)
    • (2007) Cornea , vol.26 , Issue.6 , pp. 647-649
    • Ramamurthy, B.1    Sachdeva, V.2    Mandal, A.K.3    Vemuganti, G.K.4    Garg, P.5    Sangwan, V.S.6
  • 12
    • 76149131704 scopus 로고    scopus 로고
    • High measured intraocular pressure in children with recessive congenital hereditary endothelial dystrophy
    • Khan AO, Al-Shehah A, Ghadhfan FE. High measured intraocular pressure in children with recessive congenital hereditary endothelial dystrophy. J Pediatr Ophthalmol Strabismus 2010; 47:29-33.
    • (2010) J Pediatr Ophthalmol Strabismus , vol.47 , pp. 29-33
    • Khan, A.O.1    Al-Shehah, A.2    Ghadhfan, F.E.3
  • 14
    • 0033119388 scopus 로고    scopus 로고
    • Corneal transplantation in young children with congenital hereditary endothelial dystrophy
    • DOI 10.1016/S0002-9394(98)00435-8, PII S0002939498004358
    • Schaumberg DA, Moyes AL, Gomes JA, Dana MR. Corneal transplantation in young children with congenital hereditary endothelial dystrophy. Multicenter Pediatric Keratoplasty Study. Am J Ophthalmol 1999; 127:373-378. (Pubitemid 29165469)
    • (1999) American Journal of Ophthalmology , vol.127 , Issue.4 , pp. 373-378
    • Schaumberg, D.A.1    Moyes, A.L.2    Gomes, J.A.P.3    Dana, M.R.4
  • 15
    • 84862798152 scopus 로고    scopus 로고
    • Successful Descemet's stripping automated endothelial keratoplasty for congenital hereditary endothelial dystrophy in a pediatric patient
    • Goshe JM, Li JY, Terry MA. Successful Descemet's stripping automated endothelial keratoplasty for congenital hereditary endothelial dystrophy in a pediatric patient. Int Ophthalmol 2012; 32:61-66.f
    • (2012) Int Ophthalmol , vol.32
    • Goshe, J.M.1    Li, J.Y.2    Terry, M.A.3
  • 16
    • 73449124813 scopus 로고    scopus 로고
    • Phenotypic characterisation and ZEB1 mutational analysis in posterior polymorphous corneal dystrophy in a New Zealand population
    • Vincent AL, Niederer RL, Richards A, et al. Phenotypic characterisation and ZEB1 mutational analysis in posterior polymorphous corneal dystrophy in a New Zealand population. Mol Vis 2009; 15:2544-2553.
    • (2009) Mol Vis , vol.15 , pp. 2544-2553
    • Vincent, A.L.1    Niederer, R.L.2    Richards, A.3
  • 17
    • 33144458754 scopus 로고    scopus 로고
    • A new, X-linked endothelial corneal dystrophy
    • Schmid E, Lisch W, Philipp W, et al. A new, X-linked endothelial corneal dystrophy. Am J Ophthalmol 2006; 141:478-487.
    • (2006) Am J Ophthalmol , vol.141 , pp. 478-487
    • Schmid, E.1    Lisch, W.2    Philipp, W.3
  • 18
    • 0038336520 scopus 로고    scopus 로고
    • Outcome of lamellar keratoplasty for limbal dermoids in children
    • DOI 10.1067/mpa.2002.124651
    • Watts P, Michaeli-Cohen A, Abdolell M, Rootman D. Outcome of lamellar keratoplasty for limbal dermoids in children. J AAPOS 2002; 6:209-215. (Pubitemid 36886584)
    • (2002) Journal of AAPOS , vol.6 , Issue.4 , pp. 209-215
    • Watts, P.1    Michaeli-Cohen, A.2    Abdolell, M.3    Rootman, D.4
  • 21
    • 18344399528 scopus 로고
    • Les differents types de sclerocornee leurs modes d'heredite et les malformations congenitales concomitants
    • Bloch N. Les differents types de sclerocornee, leurs modes d'heredite et les malformations congenitales concomitantes. [The different types of sclerocornea, their modes of inheritance and concomitant congenital malformations]. J Genet Hum 1965; 14:133-172.
    • (1965) J Genet Hum , vol.14 , pp. 133-172
    • Bloch, N.1
  • 22
    • 80052497392 scopus 로고    scopus 로고
    • CYP1B1-related anterior segment developmental anomalies novel mutations for infantile glaucoma and von Hippel's ulcer revisited
    • Kelberman D, Islam L, Jacques TS, et al. CYP1B1-related anterior segment developmental anomalies novel mutations for infantile glaucoma and von Hippel's ulcer revisited. Ophthalmology 2011; 118:1865-1873.
    • (2011) Ophthalmology , vol.118 , pp. 1865-1873
    • Kelberman, D.1    Islam, L.2    Jacques, T.S.3
  • 23
    • 34250697152 scopus 로고    scopus 로고
    • Long-term visual prognosis in children after corneal transplant surgery for Peters anomaly type i
    • Zaidman GW, Flanagan JK, Furey CC. Long-term visual prognosis in children after corneal transplant surgery for Peters anomaly type I. Am J Ophthalmol 2007; 144:104-108.
    • (2007) Am J Ophthalmol , vol.144 , pp. 104-108
    • Zaidman, G.W.1    Flanagan, J.K.2    Furey, C.C.3
  • 24
    • 79960698798 scopus 로고    scopus 로고
    • Peters anomaly: Review of the literature
    • Bhandari R, Ferri S, Whittaker B, et al. Peters anomaly: review of the literature. Cornea 2011; 30:939-944.
    • (2011) Cornea , vol.30 , pp. 939-944
    • Bhandari, R.1    Ferri, S.2    Whittaker, B.3
  • 25
    • 53949108516 scopus 로고    scopus 로고
    • A novel mutation in the FOXC1 gene in a family with Axenfeld-Rieger syndrome and Peters' anomaly
    • Weisschuh N, Wolf C, Wissinger B, Gramer E. A novel mutation in the FOXC1 gene in a family with Axenfeld-Rieger syndrome and Peters' anomaly. Clin Genet 2008; 74:476-480.
    • (2008) Clin Genet , vol.74 , pp. 476-480
    • Weisschuh, N.1    Wolf, C.2    Wissinger, B.3    Gramer, E.4
  • 27
    • 83455255312 scopus 로고    scopus 로고
    • Two novel mutations of the PAX6 gene causing different phenotype in a cohort of Chinese patients
    • Zhang X, Tong Y, Xu W, et al. Two novel mutations of the PAX6 gene causing different phenotype in a cohort of Chinese patients. Eye 2011; 25:1581-1589.
    • (2011) Eye , vol.25 , pp. 1581-1589
    • Zhang, X.1    Tong, Y.2    Xu, W.3
  • 30
    • 73349099376 scopus 로고    scopus 로고
    • Seeing clearly: The dominant and recessive nature of FOXE3 in eye developmental anomalies
    • Iseri SU, Osborne RJ, Farrall M, Wyatt AW, et al. Seeing clearly: the dominant and recessive nature of FOXE3 in eye developmental anomalies. Hum Mutat 2009; 30:1378-1386.
    • (2009) Hum Mutat , vol.30 , pp. 1378-1386
    • Iseri, S.U.1    Osborne, R.J.2    Farrall, M.3    Wyatt, A.W.4
  • 31
    • 77955643791 scopus 로고    scopus 로고
    • Homozygous FOXE3 mutations cause nonsyndromic, bilateral, total sclerocornea, aphakia, microphthalmia and optic disc coloboma
    • Ali M, Buentello-Volante B, McKibbin M, et al. Homozygous FOXE3 mutations cause nonsyndromic, bilateral, total sclerocornea, aphakia, microphthalmia and optic disc coloboma. Mol Vis 2010; 16:1162-1168.
    • (2010) Mol Vis , vol.16 , pp. 1162-1168
    • Ali, M.1    Buentello-Volante, B.2    McKibbin, M.3
  • 33
  • 34
    • 79952655582 scopus 로고    scopus 로고
    • A case of aniridia with unilateral Peters anomaly
    • Sawada M, Sato M, Hikoya A, et al. A case of aniridia with unilateral Peters anomaly. J AAPOS 2011; 15:104-106.
    • (2011) J AAPOS , vol.15 , pp. 104-106
    • Sawada, M.1    Sato, M.2    Hikoya, A.3
  • 35
    • 0014750863 scopus 로고
    • Changes in corneal ultrastructure resulting from early lens removal in the developing chick embryo
    • Zinn KM. Changes in corneal ultrastructure resulting from early lens removal in the developing chick embryo. Invest Ophthalmol 1970; 9:165-182.
    • (1970) Invest Ophthalmol , vol.9 , pp. 165-182
    • Zinn, K.M.1
  • 36
    • 11144244633 scopus 로고    scopus 로고
    • Corneal perforation with secondary congenital aphakia in Peters anomaly
    • DOI 10.1097/01.ico.0000134187.19117.6a
    • Banning CS, Blackmon DM, Song CD, Grossniklaus HE. Corneal perforation with secondary congenital aphakia in Peters anomaly. Cornea 2005; 24:118-120. (Pubitemid 40053508)
    • (2005) Cornea , vol.24 , Issue.1 , pp. 118-120
    • Banning, C.S.1    Blackmon, D.M.2    Song, C.D.3    Grossniklaus, H.E.4
  • 37
    • 62649111045 scopus 로고    scopus 로고
    • A clinical and molecular genetic study of German patients with primary congenital glaucoma
    • Weisschuh N, Wolf C, Wissinger B, Gramer E. A clinical and molecular genetic study of German patients with primary congenital glaucoma. Am J Ophthalmol 2009; 147:744-753.
    • (2009) Am J Ophthalmol , vol.147 , pp. 744-753
    • Weisschuh, N.1    Wolf, C.2    Wissinger, B.3    Gramer, E.4
  • 38
    • 65149084930 scopus 로고    scopus 로고
    • Null mutations in LTBP2 cause primary congenital glaucoma
    • Ali M, McKibbin M, Booth A, et al. Null mutations in LTBP2 cause primary congenital glaucoma. Am J Hum Genet 2009; 84:664-671.
    • (2009) Am J Hum Genet , vol.84 , pp. 664-671
    • Ali, M.1    McKibbin, M.2    Booth, A.3
  • 39
    • 34547581066 scopus 로고    scopus 로고
    • Bilateral congenital stromal cyst of the cornea
    • DOI 10.1016/j.jaapos.2006.12.055, PII S1091853106008068
    • Khan AO, Al-Katan H, Al-Gehedan S, Al-Rashed W. Bilateral congenital stromal cyst of the cornea. J AAPOS 2007; 11:400-401. (Pubitemid 47198501)
    • (2007) Journal of AAPOS , vol.11 , Issue.4 , pp. 400-401
    • Khan, A.O.1    Al-Katan, H.2    Al-Gehedan, S.3    Al-Rashed, W.4
  • 40
    • 80052964674 scopus 로고    scopus 로고
    • Digenic inheritance of mutations in FOXC1 and PITX2: Correlating transcription factor function and Axenfeld- Rieger disease severity
    • Kelberman D, Islam L, Holder SE, et al. Digenic inheritance of mutations in FOXC1 and PITX2: correlating transcription factor function and Axenfeld- Rieger disease severity. Hum Mutat 2011; 32:1144-1152.
    • (2011) Hum Mutat , vol.32 , pp. 1144-1152
    • Kelberman, D.1    Islam, L.2    Holder, S.E.3
  • 41
    • 81855169549 scopus 로고    scopus 로고
    • Unilateral keratitis following death of a twin as the presenting sign of herpetic infection in a neonate
    • Wang E, Schnall BM, Rotschild T, et al. Unilateral keratitis following death of a twin as the presenting sign of herpetic infection in a neonate. J AAPOS 2011; 15:489-490.
    • (2011) J AAPOS , vol.15 , pp. 489-490
    • Wang, E.1    Schnall, B.M.2    Rotschild, T.3
  • 43
    • 79960700281 scopus 로고    scopus 로고
    • Corneal autograft and allograft in a 10-month-old premature boy with acquired bilateral corneal opacities
    • Tannen B, Zarbin MA, Bhagat N, et al. Corneal autograft and allograft in a 10-month-old premature boy with acquired bilateral corneal opacities. Cornea 2011; 30:905-906.
    • (2011) Cornea , vol.30 , pp. 905-906
    • Tannen, B.1    Zarbin, M.A.2    Bhagat, N.3
  • 46
    • 78049248371 scopus 로고    scopus 로고
    • Indications and outcomes of deep anterior lamellar keratoplasty in children
    • Harding SA, Nischal KK, Upponi-Patil A, Fowler DJ. Indications and outcomes of deep anterior lamellar keratoplasty in children. Ophthalmology 2010; 117:2191-2195.
    • (2010) Ophthalmology , vol.117 , pp. 2191-2195
    • Harding, S.A.1    Nischal, K.K.2    Upponi-Patil, A.3    Fowler, D.J.4
  • 47
    • 67149111620 scopus 로고    scopus 로고
    • Descemet stripping automated endothelial keratoplasty in a child with descemet membrane breaks after forceps delivery
    • Ponchel C, Malecaze F, Arné JL, Fournié P. Descemet stripping automated endothelial keratoplasty in a child with descemet membrane breaks after forceps delivery. Cornea 2009; 28:338-341.
    • (2009) Cornea , vol.28 , pp. 338-341
    • Ponchel, C.1    Malecaze, F.2    Arné, J.L.3    Fournié, P.4
  • 48
    • 0021988360 scopus 로고
    • Treatment of corneal opacification in mucolipidosis IV with conjunctival transplantation
    • Dangel ME, Bremer DL, Rogers GL. Treatment of corneal opacification in mucolipidosis IV with conjunctival transplantation. Am J Ophthalmol 1985; 99:137-141. (Pubitemid 15119571)
    • (1985) American Journal of Ophthalmology , vol.99 , Issue.2 , pp. 137-141
    • Dangel, M.E.1    Bremer, D.L.2    Rogers, G.L.3
  • 49
    • 49849084978 scopus 로고    scopus 로고
    • Outcome of penetrating keratoplasty for Peters anomaly
    • Rao KV, Fernandes M, Gangopadhyay N, Vemuganti GK, et al. Outcome of penetrating keratoplasty for Peters anomaly. Cornea 2008; 27:749-753.
    • (2008) Cornea , vol.27 , pp. 749-753
    • Rao, K.V.1    Fernandes, M.2    Gangopadhyay, N.3    Vemuganti, G.K.4
  • 51
    • 0033511472 scopus 로고    scopus 로고
    • Long-term results of corneal graft survival in infants and children with Peters anomaly
    • Yang LL, Lambert SR, Lynn MJ, Stulting RD. Long-term results of corneal graft survival in infants and children with Peters anomaly. Ophthalmology 1999; 106:833-848. (Pubitemid 30194331)
    • (1999) Ophthalmology , vol.106 , Issue.4 , pp. 833-848
    • Yang, L.L.H.1    Lambert, S.R.2    Lynn, M.J.3    Stulting, R.D.4
  • 52
    • 0031452727 scopus 로고    scopus 로고
    • Corneal transplantation in children with Peters anomaly and mesenchymal dysgeneses
    • Dana MR, Schaumberg DA, Moyes AL, Gomes JA. Corneal transplantation in children with Peters anomaly and mesenchymal dysgenesis. Multicenter Pediatric Keratoplasty Study. Ophthalmology 1997; 104:1580-1586. (Pubitemid 28053454)
    • (1997) Ophthalmology , vol.104 , Issue.10 , pp. 1580-1586
    • Dana, M.R.1    Scaumberg, D.A.2    Moyes, A.L.3    Gomes, J.A.P.4    Stark, W.J.5
  • 53
    • 0036729453 scopus 로고    scopus 로고
    • Developmental outcome, including setback, in young children with severe visual impairment
    • DOI 10.1017/S0012162201002651
    • Dale N, Sonksen P. Developmental outcome, including setback, in young children with severe visual impairment. Dev Med Child Neurol 2002; 44:613-622. (Pubitemid 34987633)
    • (2002) Developmental Medicine and Child Neurology , vol.44 , Issue.9 , pp. 613-622
    • Dale, N.1    Sonksen, P.2
  • 54
    • 0020694508 scopus 로고
    • The assessment of 'vision for development' in severely visually handicapped babies
    • Sonksen PM. The assessment of 'vision for development' in severely visually handicapped babies. Acta Ophthalmol Suppl 1983; 157:82-90. (Pubitemid 13194564)
    • (1983) Acta Ophthalmologica , vol.61 , Issue.SUPPL. 157 , pp. 82-90
    • Sonksen, P.M.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.