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Volumn 123, Issue 1, 1997, Pages 97-99

Congenital conductive hearing loss in the lacrimoauriculodentodigital syndrome

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; CASE REPORT; CLINICAL FEATURE; CONDUCTION DEAFNESS; EAR MALFORMATION; FEMALE; HUMAN; ORAL SURGERY; SCHOOL CHILD; SKELETON MALFORMATION; STAPEDECTOMY; THUMB MALFORMATION;

EID: 0031037605     PISSN: 08864470     EISSN: None     Source Type: Journal    
DOI: 10.1001/archotol.1997.01900010107017     Document Type: Article
Times cited : (11)

References (14)
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    • Levy WJ. Mesoectodermal dysplasia: a new combination of abnormalities. Am J Ophthalmol. 1969; 63:978-982.
    • (1969) Am J Ophthalmol , vol.63 , pp. 978-982
    • Levy, W.J.1
  • 4
    • 0014399820 scopus 로고
    • Familial microtia with meatal atresia in two sibships
    • Ellwood LC, Winter ST, Dar H. Familial microtia with meatal atresia in two sibships. J Med Genet. 1968;5:289-291.
    • (1968) J Med Genet , vol.5 , pp. 289-291
    • Ellwood, L.C.1    Winter, S.T.2    Dar, H.3
  • 6
    • 0014489279 scopus 로고
    • Conductive hearing loss and malformed low set ears as a possible recessive syndrome
    • Mengel MC, Koningsmark BW, Berlin CI, McKusick VA. Conductive hearing loss and malformed low set ears as a possible recessive syndrome. J Med Genet. 1969;6:14-21.
    • (1969) J Med Genet , vol.6 , pp. 14-21
    • Mengel, M.C.1    Koningsmark, B.W.2    Berlin, C.I.3    McKusick, V.A.4
  • 8
    • 0025836623 scopus 로고
    • Congenital conductive or mixed deafness, pre-auricular sinus, external ear anomaly, commissural lip pits: An autosomal dominant inherited syndrome
    • Marres HAM, Cremers CWRJ. Congenital conductive or mixed deafness, pre-auricular sinus, external ear anomaly, commissural lip pits: an autosomal dominant inherited syndrome. Ann Otol Rhinol Laryngol. 1991;100:928-932.
    • (1991) Ann Otol Rhinol Laryngol , vol.100 , pp. 928-932
    • Marres, H.A.M.1    Cremers, C.W.R.J.2
  • 9
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    • EEC syndrome: Report on 20 new patients, clinical and genetic considerations
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    • (1990) Am J Med Genet , vol.37 , pp. 42-53
    • Rodini, E.S.O.1    Richieri-Costa, A.2
  • 10
    • 0018950468 scopus 로고
    • The IVIC syndrome: A new autosomal dominant complex pleiotropic syndrome with radial ray hypoplasia, hearing impairment, external ophthalmoplegia and thrombocytopenia
    • Arias S, Penchaszadeh VB, Pinto-Cisternas J, Larrauri S. The IVIC syndrome: a new autosomal dominant complex pleiotropic syndrome with radial ray hypoplasia, hearing impairment, external ophthalmoplegia and thrombocytopenia. Am J Med Genet. 1980;6:25-59.
    • (1980) Am J Med Genet , vol.6 , pp. 25-59
    • Arias, S.1    Penchaszadeh, V.B.2    Pinto-Cisternas, J.3    Larrauri, S.4
  • 11
    • 0017683776 scopus 로고
    • The lacrimo-auriculodento-digital syndrome
    • Shiang EL, Holmes LB. The lacrimo-auriculodento-digital syndrome. Pediatrics. 1977;59:927-930.
    • (1977) Pediatrics , vol.59 , pp. 927-930
    • Shiang, E.L.1    Holmes, L.B.2
  • 12
    • 0022591768 scopus 로고
    • LADD syndrome: Report of new cases and review of the clinical spectrum
    • Wiedemann HR, Drechser J. LADD syndrome: report of new cases and review of the clinical spectrum. Eur J Pediatr. 1986;144:579-582.
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    • Wiedemann, H.R.1    Drechser, J.2
  • 13
    • 0021995034 scopus 로고
    • Phenotypic variation in the LADD syndrome
    • Thompson E, Pembry M, Graham J. Phenotypic variation in the LADD syndrome. J Med Genet. 1985;22:382-385.
    • (1985) J Med Genet , vol.22 , pp. 382-385
    • Thompson, E.1    Pembry, M.2    Graham, J.3
  • 14
    • 0029970946 scopus 로고    scopus 로고
    • Ossicular reconstruction in cases of absent or inadequate incus, congenital malformations of the middle ear and epitympanic fixation of the incus and malleus
    • Tange RA. Ossicular reconstruction in cases of absent or inadequate incus, congenital malformations of the middle ear and epitympanic fixation of the incus and malleus. ORL J Otorhinolaryngol Relat Spec. 1996;58:143-146.
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    • Tange, R.A.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.