메뉴 건너뛰기




Volumn 78, Issue 1, 2000, Pages 101-103

Atrial septal defect with interatrial aneurysm and Axenfeld-Rieger syndrome

Author keywords

Atrial septal defect; Axenfeld Rieger syndrome; Interatrial aneurysm; Secondary glaucoma

Indexed keywords

ADULT; ANEURYSM; ARTICLE; BRAIN EMBOLISM; CARDIOVASCULAR SYSTEM EXAMINATION; CASE REPORT; DEVICE; ECHOCARDIOGRAPHY; FACE DYSMORPHIA; FEMALE; GONIOSCOPY; HEART ATRIUM SEPTUM DEFECT; HUMAN; IRIS ATROPHY; PRIORITY JOURNAL; RIEGER SYNDROME; SECONDARY GLAUCOMA; SLIT LAMP; TONOMETER;

EID: 0342948782     PISSN: 13953907     EISSN: None     Source Type: Journal    
DOI: 10.1034/j.1600-0420.2000.078001101.x     Document Type: Article
Times cited : (22)

References (15)
  • 2
    • 6844251598 scopus 로고    scopus 로고
    • Familial Axenfeld-Rieger anomaly, atrial septal defect, and sensorineural hearing loss a possible new genetic syndrome
    • Cunningham ET, Eliott D, Miller NR, Maumenee IH & Green R (1998): Familial Axenfeld-Rieger anomaly, atrial septal defect, and sensorineural hearing loss a possible new genetic syndrome. Arch Ophthalmol 116: 78-82.
    • (1998) Arch Ophthalmol , vol.116 , pp. 78-82
    • Cunningham, E.T.1    Eliott, D.2    Miller, N.R.3    Maumenee, I.H.4    Green, R.5
  • 3
    • 0015597285 scopus 로고
    • Deletion from the long arm of chromosome 4 (46, XX, 4q-) associated with congenital anomalies
    • Golbus MS, Conte FA & Daentl DL (1973): Deletion from the long arm of chromosome 4 (46, XX, 4q-) associated with congenital anomalies. J Med Genet 10: 83-85.
    • (1973) J Med Genet , vol.10 , pp. 83-85
    • Golbus, M.S.1    Conte, F.A.2    Daentl, D.L.3
  • 4
    • 0013807346 scopus 로고
    • Un cas d'embryotoxon posterieur avec buphthalmie et malformation cardiaque
    • Haye C & Blanck C (1965): Un cas d'embryotoxon posterieur avec buphthalmie et malformation cardiaque. Arch Ophthalmol (Paris), 25: 621-624.
    • (1965) Arch Ophthalmol (Paris) , vol.25 , pp. 621-624
    • Haye, C.1    Blanck, C.2
  • 5
    • 0343304811 scopus 로고    scopus 로고
    • Maggio Regione Emilia Romagna, Gruppo IMER
    • IMER Newsletter 17 (Maggio 1997), Regione Emilia Romagna, Gruppo IMER.
    • (1997) IMER Newsletter 17 , vol.17
  • 7
    • 0031820201 scopus 로고    scopus 로고
    • Cardiovascular anomaly in Rieger Syndrome: Heterogeneity or contiguity?
    • Mammi I, De Giorgio P, Clementi M & Tenconi R (1998): Cardiovascular anomaly in Rieger Syndrome: Heterogeneity or contiguity? Acta Ophthalmol Scand 76: 509-512.
    • (1998) Acta Ophthalmol Scand , vol.76 , pp. 509-512
    • Mammi, I.1    De Giorgio, P.2    Clementi, M.3    Tenconi, R.4
  • 9
    • 0025016455 scopus 로고
    • Improved morphologic characterization of atrial septal aneurysm by transesophageal echocardiography: Relation to cerebrovascular events
    • Schneider B, Hanrath P, Vogel P & Meinertz T (1990): Improved morphologic characterization of atrial septal aneurysm by transesophageal echocardiography: relation to cerebrovascular events. J Am Coll Cardiol 16: 1000-1006.
    • (1990) J Am Coll Cardiol , vol.16 , pp. 1000-1006
    • Schneider, B.1    Hanrath, P.2    Vogel, P.3    Meinertz, T.4
  • 11
    • 0025082259 scopus 로고
    • Association of cephalic neural crest cells with cardiovascular development, particularly that of the semilunar valves
    • Takamura K, Okishima T, Ohdo S & Hayakawa K (1990): Association of cephalic neural crest cells with cardiovascular development, particularly that of the semilunar valves. Anat Embryol 182: 263-272.
    • (1990) Anat Embryol , vol.182 , pp. 263-272
    • Takamura, K.1    Okishima, T.2    Ohdo, S.3    Hayakawa, K.4
  • 12
    • 0028142341 scopus 로고
    • Cardiac valvular disease and Axenfeld-Rieger syndrome
    • Tsai JC & Grajewski AL (1994): Cardiac valvular disease and Axenfeld-Rieger syndrome. Am J Ophthalmol 118: 255-256.
    • (1994) Am J Ophthalmol , vol.118 , pp. 255-256
    • Tsai, J.C.1    Grajewski, A.L.2
  • 13
    • 0029852490 scopus 로고    scopus 로고
    • Autosomal-dominant iridogoniodysgenesis and Axenfeld-Rieger syndrome are genetically distinct
    • Walter MA, Mirzayans F, Mears AJ, Hickey K & Pearce WG (1996): Autosomal-dominant iridogoniodysgenesis and Axenfeld-Rieger syndrome are genetically distinct. Ophthalmology 103: 1907-1915.
    • (1996) Ophthalmology , vol.103 , pp. 1907-1915
    • Walter, M.A.1    Mirzayans, F.2    Mears, A.J.3    Hickey, K.4    Pearce, W.G.5
  • 14
  • 15
    • 0342869789 scopus 로고
    • Dysgenesis mesodermalis cornea et iridis
    • Zygulska-Machowa H (1964): Dysgenesis mesodermalis cornea et iridis. Klin Oczna 34: 153-158.
    • (1964) Klin Oczna , vol.34 , pp. 153-158
    • Zygulska-Machowa, H.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.