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Volumn 24, Issue 1, 2005, Pages 112-115

Lattice dystrophy-like localized amyloidosis of the cornea secondary to trichiasis

Author keywords

Amyloidosis; Diagnosis; Lattice dystrophy; TGFBI

Indexed keywords

AMYLOID; TRANSFORMING GROWTH FACTOR BETA;

EID: 11144241602     PISSN: 02773740     EISSN: None     Source Type: Journal    
DOI: 10.1097/01.ico.0000134194.71981.ab     Document Type: Review
Times cited : (28)

References (26)
  • 2
    • 0027383887 scopus 로고
    • Spheroidal keratopathy associated with subepithelial corneal amyloidosis. A clinicopathologic case report and a proposed new classification for spheroidal keratopathy
    • Santo RM, Yamaguchi T, Kanai A. Spheroidal keratopathy associated with subepithelial corneal amyloidosis. A clinicopathologic case report and a proposed new classification for spheroidal keratopathy. Ophthalmology. 1993;100:1455-1461.
    • (1993) Ophthalmology , vol.100 , pp. 1455-1461
    • Santo, R.M.1    Yamaguchi, T.2    Kanai, A.3
  • 4
  • 5
    • 0042706546 scopus 로고    scopus 로고
    • Localised corneal amyloidosis associated with herpetic keratitis
    • Tejwani D, Azuara-Blanco A, MacKenzie J. Localised corneal amyloidosis associated with herpetic keratitis. Br J Ophthalmol. 2003;87:1049.
    • (2003) Br J Ophthalmol , vol.87 , pp. 1049
    • Tejwani, D.1    Azuara-Blanco, A.2    MacKenzie, J.3
  • 6
    • 0023930957 scopus 로고
    • Corneal amyloidosis associated with keratoconus
    • Stern GA, Knapp A, Hood CI. Corneal amyloidosis associated with keratoconus. Ophthalmology. 1988;95:52-55.
    • (1988) Ophthalmology , vol.95 , pp. 52-55
    • Stern, G.A.1    Knapp, A.2    Hood, C.I.3
  • 7
    • 0031020733 scopus 로고    scopus 로고
    • Kerato-epithelin mutations in four 5q31-linked corneal dystrophies
    • Munier FL, Korvatska E, Djemai A, et al. Kerato-epithelin mutations in four 5q31-linked corneal dystrophies. Nature Genet. 1997;15:247-251.
    • (1997) Nature Genet , vol.15 , pp. 247-251
    • Munier, F.L.1    Korvatska, E.2    Djemai, A.3
  • 8
    • 0032407550 scopus 로고    scopus 로고
    • Gelatinous drop-like corneal dystrophy is not one of the beta ig-h3-mutated corneal amyloidoses
    • Dota A, Nishida K, Honma Y, et al. Gelatinous drop-like corneal dystrophy is not one of the beta ig-h3-mutated corneal amyloidoses. Am J Ophthalmol. 1998;126:832-833.
    • (1998) Am J Ophthalmol , vol.126 , pp. 832-833
    • Dota, A.1    Nishida, K.2    Honma, Y.3
  • 9
    • 0032900158 scopus 로고    scopus 로고
    • Identification of the gene responsible for gelatinous drop-like corneal dystrophy
    • Tsujikawa M, Kurahashi H, Tanaka T, et al. Identification of the gene responsible for gelatinous drop-like corneal dystrophy. Nature Genet. 1999;21:420-423.
    • (1999) Nature Genet , vol.21 , pp. 420-423
    • Tsujikawa, M.1    Kurahashi, H.2    Tanaka, T.3
  • 10
    • 0038312068 scopus 로고    scopus 로고
    • Localized amyloidosis of the cornea secondary to trichiasis: Clinical course and pathogenesis
    • Lin PY, Kao SC, Hsueh KF, et al. Localized amyloidosis of the cornea secondary to trichiasis: clinical course and pathogenesis. Cornea. 2003;22:491-494.
    • (2003) Cornea , vol.22 , pp. 491-494
    • Lin, P.Y.1    Kao, S.C.2    Hsueh, K.F.3
  • 11
    • 0033462204 scopus 로고    scopus 로고
    • Advances in the molecular genetics of corneal dystrophies
    • Klintworth G. Advances in the molecular genetics of corneal dystrophies. Am J Ophthalmol. 1999;128:747-754.
    • (1999) Am J Ophthalmol , vol.128 , pp. 747-754
    • Klintworth, G.1
  • 12
    • 0036218069 scopus 로고    scopus 로고
    • Distichiasis, trichiasis, and entropion: Advances in management
    • Choo PH. Distichiasis, trichiasis, and entropion: advances in management. Int Ophthalmol Clin. 2002;42:75-87.
    • (2002) Int Ophthalmol Clin , vol.42 , pp. 75-87
    • Choo, P.H.1
  • 13
    • 0015450418 scopus 로고
    • Congenital distichiasis. A report of eleven cases and an investigation of the mode of inheritance
    • Mustonen E. Congenital distichiasis. A report of eleven cases and an investigation of the mode of inheritance. Acta Ophthalmol (Copenh). 1972;50:598-607.
    • (1972) Acta Ophthalmol (Copenh) , vol.50 , pp. 598-607
    • Mustonen, E.1
  • 14
    • 0023265419 scopus 로고
    • Secondary localized amyloidosis of the cornea caused by trichiasis
    • Hayasaka S, Setogawa T, Ohmura M. Secondary localized amyloidosis of the cornea caused by trichiasis. Ophthalmologica. 1987;194:77-81.
    • (1987) Ophthalmologica , vol.194 , pp. 77-81
    • Hayasaka, S.1    Setogawa, T.2    Ohmura, M.3
  • 15
    • 0029901641 scopus 로고    scopus 로고
    • A histopathological study of corneal amyloidosis secondary to trichiasis
    • Kigasawa K, Mashima Y, Ogata T, et al. [A histopathological study of corneal amyloidosis secondary to trichiasis]. Nippon Ganka Gakkai Zasshi. 1996;100:394-400.
    • (1996) Nippon Ganka Gakkai Zasshi , vol.100 , pp. 394-400
    • Kigasawa, K.1    Mashima, Y.2    Ogata, T.3
  • 16
    • 0030135925 scopus 로고    scopus 로고
    • Characteristic distribution of deposits in recurrent granular corneal dystrophy
    • Auw-Haedrich C, Loeffler KU, Sundmacher R, et al. Characteristic distribution of deposits in recurrent granular corneal dystrophy. Ger J Ophthalmol. 1996;5:132-136.
    • (1996) Ger J Ophthalmol , vol.5 , pp. 132-136
    • Auw-Haedrich, C.1    Loeffler, K.U.2    Sundmacher, R.3
  • 17
    • 0033818425 scopus 로고    scopus 로고
    • Genetics of the corneal dystrophies: What we have learned in the past twenty-five years
    • Bron AJ. Genetics of the corneal dystrophies: what we have learned in the past twenty-five years. Cornea. 2000;19:699-711.
    • (2000) Cornea , vol.19 , pp. 699-711
    • Bron, A.J.1
  • 18
    • 0028143362 scopus 로고
    • Granular corneal dystrophy. Visual results and pattern of recurrence after lamellar or penetrating keratoplasty
    • Lyons CJ, McCartney AC, Kirkness CM, et al. Granular corneal dystrophy. Visual results and pattern of recurrence after lamellar or penetrating keratoplasty. Ophthalmology. 1994;101:1812-1817.
    • (1994) Ophthalmology , vol.101 , pp. 1812-1817
    • Lyons, C.J.1    McCartney, A.C.2    Kirkness, C.M.3
  • 19
    • 0033003369 scopus 로고    scopus 로고
    • Deposits and proteoglycan changes in primary and recurrent granular dystrophy of the cornea
    • Akhtar S, Meek KM, Ridgway AE, et al. Deposits and proteoglycan changes in primary and recurrent granular dystrophy of the cornea. Arch Ophthalmol. 1999;117:310-321.
    • (1999) Arch Ophthalmol , vol.117 , pp. 310-321
    • Akhtar, S.1    Meek, K.M.2    Ridgway, A.E.3
  • 20
    • 0025967791 scopus 로고
    • Climatic droplet keratopathy with corneal amyloidosis
    • Malta CS, Tabbara KF, Cameron JA, et al. Climatic droplet keratopathy with corneal amyloidosis. Ophthalmology. 1991;98:192-195.
    • (1991) Ophthalmology , vol.98 , pp. 192-195
    • Malta, C.S.1    Tabbara, K.F.2    Cameron, J.A.3
  • 21
    • 0015055804 scopus 로고
    • Unilateral lattice dystrophy of the cornea. Report of a case
    • Reshmi CS. Unilateral lattice dystrophy of the cornea. Report of a case. Med J Aust. 1971;1:966-967.
    • (1971) Med J Aust , vol.1 , pp. 966-967
    • Reshmi, C.S.1
  • 22
    • 0018842922 scopus 로고
    • Unilateral lattice dystrophy of the cornea
    • Mehta RF. Unilateral lattice dystrophy of the cornea. Br J Ophthalmol. 1980;64:53-55.
    • (1980) Br J Ophthalmol , vol.64 , pp. 53-55
    • Mehta, R.F.1
  • 24
    • 0033498186 scopus 로고    scopus 로고
    • A mutation within exon 14 of the TGFBI (BIGH3) gene on chromosome 5q31 causes an asymmetric, late-onset form of lattice corneal dystrophy
    • Stewart H, Black GC, Donnai D, et al. A mutation within exon 14 of the TGFBI (BIGH3) gene on chromosome 5q31 causes an asymmetric, late-onset form of lattice corneal dystrophy. Ophthalmology. 1999;106:964-970.
    • (1999) Ophthalmology , vol.106 , pp. 964-970
    • Stewart, H.1    Black, G.C.2    Donnai, D.3
  • 25
    • 0034972072 scopus 로고    scopus 로고
    • Late-onset form of lattice corneal dystrophy caused by leu527Arg mutation of the TGFBI gene
    • Hirano K, Hotta Y, Nakamura M, et al. Late-onset form of lattice corneal dystrophy caused by leu527Arg mutation of the TGFBI gene. Cornea. 2001;20:525-529.
    • (2001) Cornea , vol.20 , pp. 525-529
    • Hirano, K.1    Hotta, Y.2    Nakamura, M.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.