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Volumn 1, Issue 3, 1997, Pages 180-182

Congenital iris ectropion associated with ocular albinism, foveal hypoplasia, and keratoconjunctivitis sicca

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CASE REPORT; CONGENITAL MALFORMATION; EYE MALFORMATION; FEMALE; HUMAN; IRIS; KERATOCONJUNCTIVITIS SICCA; OCULAR ALBINISM; PATHOLOGY; PIGMENT EPITHELIUM; PRESCHOOL CHILD; RETINA FOVEA; VISUAL ACUITY;

EID: 0031215959     PISSN: 10918531     EISSN: None     Source Type: Journal    
DOI: 10.1016/S1091-8531(97)90063-X     Document Type: Article
Times cited : (3)

References (8)
  • 1
    • 0025189563 scopus 로고
    • Congenital iris ectropion and a new classification for anterior segment dysgenesis
    • Wilson ME. Congenital iris ectropion and a new classification for anterior segment dysgenesis. J Pediatr Ophthalmol Strabismus 1990;27:46-55.
    • (1990) J Pediatr Ophthalmol Strabismus , vol.27 , pp. 46-55
    • Wilson, M.E.1
  • 2
    • 0021877686 scopus 로고
    • Primary glaucoma associated with iridotrabecular dysgenesis and ectropion uveae
    • Dowling JL, Albert DM, Nelson LB, Walton DS. Primary glaucoma associated with iridotrabecular dysgenesis and ectropion uveae. Ophthalmology 1985;92:912-91.
    • (1985) Ophthalmology , vol.92 , pp. 912-991
    • Dowling, J.L.1    Albert, D.M.2    Nelson, L.B.3    Walton, D.S.4
  • 3
    • 0022411638 scopus 로고
    • Ectropion congénital de l'épithélium irien et glaucome
    • Béchetoille A, Ebran JM, Bigorgne J. Ectropion congénital de l'épithélium irien et glaucome. J Fr Ophtalmol 1985;8:529-34.
    • (1985) J Fr Ophtalmol , vol.8 , pp. 529-534
    • Béchetoille, A.1    Ebran, J.M.2    Bigorgne, J.3
  • 4
    • 0022794655 scopus 로고
    • Aniridia, congenital glaucoma, and hydrocephalus in a male infant with ring chromosome 6
    • Levin H. Aniridia, congenital glaucoma, and hydrocephalus in a male infant with ring chromosome 6. Am J Med Genet 1986;25:281-7.
    • (1986) Am J Med Genet , vol.25 , pp. 281-287
    • Levin, H.1
  • 6
    • 0022609038 scopus 로고
    • Coexistence of Prader-Willi syndrome, congenital ectropion uveae with glaucoma, and factor XI deficiency
    • Futterweit W, Ritch R, Teekhasaenee C, Nelson ES. Coexistence of Prader-Willi syndrome, congenital ectropion uveae with glaucoma, and factor XI deficiency. JAMA 1986;255:3280-2.
    • (1986) JAMA , vol.255 , pp. 3280-3282
    • Futterweit, W.1    Ritch, R.2    Teekhasaenee, C.3    Nelson, E.S.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.