메뉴 건너뛰기




Volumn 242, Issue 6, 2004, Pages 495-500

Ocular symptoms and signs in patients with ectodermal dysplasia syndromes

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; AGED; ARTICLE; BASAL CELL NEVUS SYNDROME; CASE STUDY; CHILD; CLINICAL ARTICLE; CLINICAL FEATURE; CLINICAL OBSERVATION; CONTROLLED STUDY; CORNEA DISEASE; DIAGNOSTIC PROCEDURE; DISEASE SEVERITY; DRY EYE; ECTODERMAL DYSPLASIA; ECTRODACTYLY; EYE DISEASE; EYEBROW; EYELASH; FEMALE; HUMAN; HYPOHIDROTIC ECTODERMAL DYSPLASIA; INFANT; MEIBOMIAN GLAND; OPHTHALMOLOGY; OUTCOMES RESEARCH; PANNUS; PRIORITY JOURNAL; RELIABILITY; SYMPTOMATOLOGY; VISUAL SYSTEM EXAMINATION;

EID: 3142602170     PISSN: 0721832X     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00417-004-0868-0     Document Type: Article
Times cited : (68)

References (23)
  • 2
    • 0013455952 scopus 로고
    • Mendelian inheritance in man. Catalogs of autosomal dominant, autosomal recessive and x-linked phenotypes
    • The John Hopkins University Press, Baltimore, 137, 215-217, 1784, 1816-1817
    • McKusick V (1988) Mendelian inheritance in man. Catalogs of autosomal dominant, autosomal recessive and x-linked phenotypes. The John Hopkins University Press, Baltimore, pp 137, 215-217, 1784, 1816-1817, 3404-3406
    • (1988) , pp. 3404-3406
    • McKusick, V.1
  • 3
    • 85039499446 scopus 로고    scopus 로고
    • www.nfed.org/nfedserv.htm
    • www.nfed.org/nfedserv.htm
  • 5
    • 0022385395 scopus 로고
    • Keratopathy in a family with ectrodactyly-ectodermal dysplasia-clefting syndrome
    • Mawhorter LG, Ruttum MS, Koenig SB (1985) Keratopathy in a family with ectrodactyly-ectodermal dysplasia-clefting syndrome. Ophthalmology 92:1427-1431
    • (1985) Ophthalmology , vol.92 , pp. 1427-1431
    • Mawhorter, L.G.1    Ruttum, M.S.2    Koenig, S.B.3
  • 8
    • 0021356491 scopus 로고
    • Absent meibomian glands in the ectrodactyly, ectodermal dysplasia, cleft lip-palate syndrome
    • Mondino BJ, Bath PE, Foos RY et al (1984) Absent meibomian glands in the ectrodactyly, ectodermal dysplasia, cleft lip-palate syndrome. Am J Ophthalmol 97:496-500
    • (1984) Am. J. Ophthalmol. , vol.97 , pp. 496-500
    • Mondino, B.J.1    Bath, P.E.2    Foos, R.Y.3
  • 9
    • 0031879474 scopus 로고    scopus 로고
    • Ophthalmic manifestations of ectrodactyly-ectodermal dysplasia-clefting syndrome
    • Ireland IA, Meyer DR (1998) Ophthalmic manifestations of ectrodactyly-ectodermal dysplasia-clefting syndrome. Ophthalmic Plast Reconstr Surg 14:295-297
    • (1998) Ophthalmic. Plast. Reconstr. Surg. , vol.14 , pp. 295-297
    • Ireland, I.A.1    Meyer, D.R.2
  • 10
    • 0026377021 scopus 로고
    • Meibomian gland disease. Classification and grading of lid changes
    • Bron AJ, Benjamin L, Snibson GR (1991) Meibomian gland disease. Classification and grading of lid changes. Eye 5:395-411
    • (1991) Eye , vol.5 , pp. 395-411
    • Bron, A.J.1    Benjamin, L.2    Snibson, G.R.3
  • 11
    • 0022347721 scopus 로고
    • In vivo transillumination biomicroscopy and photography of meibomian gland dysfunction. A clinical study
    • Robin JB, Jester JV, Nobe J et al (1985) In vivo transillumination biomicroscopy and photography of meibomian gland dysfunction. A clinical study. Ophthalmology 92:1423-1426
    • (1985) Ophthalmology , vol.92 , pp. 1423-1426
    • Robin, J.B.1    Jester, J.V.2    Nobe, J.3
  • 12
    • 0023230573 scopus 로고
    • Hypohidrotic ectodermal dysplasia
    • Clarke A (1987) Hypohidrotic ectodermal dysplasia. J Med Genet 24:659-663
    • (1987) J. Med. Genet. , vol.24 , pp. 659-663
    • Clarke, A.1
  • 13
    • 0042169496 scopus 로고
    • Congenital ectodermal defect, with report of a case
    • Goeckermann WH (1920) Congenital ectodermal defect, with report of a case. Arch Syph Dermatol 1:396-412
    • (1920) Arch. Syph. Dermatol. , vol.1 , pp. 396-412
    • Goeckermann, W.H.1
  • 14
    • 0002760563 scopus 로고
    • A hereditary ectodermal dystrophy
    • Clouston HR (1929) A hereditary ectodermal dystrophy. Can Med Ass J 21:18-31
    • (1929) Can. Med. Ass. J. , vol.21 , pp. 18-31
    • Clouston, H.R.1
  • 15
    • 0009431171 scopus 로고
    • Hereditary ectodermal dysplasia (congenital ectodermal defect). A report of two cases
    • Weech AA (1928) Hereditary ectodermal dysplasia (congenital ectodermal defect). A report of two cases. Am J Dis Child 37:766-790
    • (1928) Am. J. Dis. Child , vol.37 , pp. 766-790
    • Weech, A.A.1
  • 16
    • 3543033174 scopus 로고
    • Hereditary ectodermal dysplasia. Report of a case, with experimental study
    • Felsher Z (1944) Hereditary ectodermal dysplasia. Report of a case, with experimental study. Arch Dermatol Syph 49:410-414
    • (1944) Arch. Dermatol. Syph. , vol.49 , pp. 410-414
    • Felsher, Z.1
  • 17
    • 0016276451 scopus 로고
    • Ocular manifestations of the ectrodactyly, ectodermal dyplasia, cleft lip-palate syndrome
    • Baum JL, Bull MJ (1974) Ocular manifestations of the ectrodactyly, ectodermal dyplasia, cleft lip-palate syndrome. Am J Ophthalmol 78:211-216
    • (1974) Am. J. Ophthalmol. , vol.78 , pp. 211-216
    • Baum, J.L.1    Bull, M.J.2
  • 18
    • 85039501552 scopus 로고    scopus 로고
    • Klinische Untersuchung zur Verweildauer und Wirkdauer von Liposic AT bei Keratokonjunktivitis sicca
    • Torens S, Berger E, Stave J, Guthoff R (2000) Klinische Untersuchung zur Verweildauer und Wirkdauer von Liposic AT bei Keratokonjunktivitis sicca. Ophthalmologe 97:S55
    • (2000) Ophthalmologe , vol.97
    • Torens, S.1    Berger, E.2    Stave, J.3    Guthoff, R.4
  • 19
    • 0019789469 scopus 로고
    • The effect of various intakes of ω-3-fatty acids on the blood lipid composition in healthy human subjects
    • Bronsgeest-Schoute HC, van Gent CM, Luten JB, Ruiter A (1981) The effect of various intakes of ω-3-fatty acids on the blood lipid composition in healthy human subjects. Am J Clin Nutr 34:1752-1757
    • (1981) Am. J. Clin. Nutr. , vol.34 , pp. 1752-1757
    • Bronsgeest-Schoute, H.C.1    van Gent, C.M.2    Luten, J.B.3    Ruiter, A.4
  • 20
    • 0026671579 scopus 로고
    • EEC syndrome is on 7q11.2-q21.3
    • Letter
    • Qumsiyeh M (1992) EEC syndrome is on 7q11.2-q21.3. Letter. Clin Genet 42:101
    • (1992) Clin. Genet. , vol.42 , pp. 101
    • Qumsiyeh, M.1
  • 21
    • 0027199727 scopus 로고
    • The breakpoints of the EEC Syndrome (ectrodactyly, ectodermal dysplasia and cleft lip/palate) confirmed to 7q11.21 and 9p12 by fluorescence in situ hybridization
    • Letter
    • Fukushima Y, Ohashi H, Hasegawa T (1993): The breakpoints of the EEC Syndrome (ectrodactyly, ectodermal dysplasia and cleft lip/palate) confirmed to 7q11.21 and 9p12 by fluorescence in situ hybridization. Letter. Clin Genet 44:50
    • (1993) Clin. Genet. , vol.44 , pp. 50
    • Fukushima, Y.1    Ohashi, H.2    Hasegawa, T.3
  • 22
    • 12644310324 scopus 로고    scopus 로고
    • The Tabby phenotype is caused by mutation in a mouse homologue of the EDA gene that reveals novel mouse and human exons and encodes a protein (ectodysplasin-A) with collagenous domains
    • Srivastava A, Pispa J, Hartung A et al (1997) The Tabby phenotype is caused by mutation in a mouse homologue of the EDA gene that reveals novel mouse and human exons and encodes a protein (ectodysplasin-A) with collagenous domains. Proc Natl Acad Sci USA 94:13069-13074
    • (1997) Proc. Natl. Acad. Sci. USA , vol.94 , pp. 13069-13074
    • Srivastava, A.1    Pispa, J.2    Hartung, A.3
  • 23
    • 0025351528 scopus 로고
    • Induction of sweat glands by epidermal growth factor in murine x-linked anhidrotic ectodermal dysplasia
    • Blecher SR, Kapalanga J, Lalonde D (1990) Induction of sweat glands by epidermal growth factor in murine x-linked anhidrotic ectodermal dysplasia. Nature 345:542-544
    • (1990) Nature , vol.345 , pp. 542-544
    • Blecher, S.R.1    Kapalanga, J.2    Lalonde, D.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.