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Volumn 5, Issue 6, 2002, Pages 592-596

Newborn with anophthalmia and features of Fryns syndrome

Author keywords

Bilateral anophthalmia; Diaphragmatic hernia; Fryns syndrome

Indexed keywords

ACCESSORY SPLEEN; ANOPHTHALMIA; ARTICLE; AUTOPSY; CASE REPORT; CORNEA DISEASE; CRANIOFACIAL MALFORMATION; DIAPHRAGM HERNIA; DIFFERENTIAL DIAGNOSIS; EAR MALFORMATION; FEMALE; FRYNS SYNDROME; HAND MALFORMATION; HUMAN; LUNG HYPOPLASIA; MATTHEW WOOD SYNDROME; NECK; NEWBORN; OPTIC NERVE HYPOPLASIA; PRIORITY JOURNAL; SYNDROME;

EID: 0036878770     PISSN: 10935266     EISSN: None     Source Type: Journal    
DOI: 10.1007/s10024-002-2106-2     Document Type: Article
Times cited : (10)

References (16)
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  • 3
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    • Pulmonary agenesis, microphthalmia, and diaphragmatic defect (PMD): New syndrome or association?
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  • 6
    • 0029781606 scopus 로고    scopus 로고
    • Use of three-dimensional ultrasound to establish the prenatal diagnosis of Fryns syndrome
    • Wymersch DV, Favre R, Gasser B. Use of three-dimensional ultrasound to establish the prenatal diagnosis of Fryns syndrome. Fetal Diagn Ther 1996;11:335-340.
    • (1996) Fetal Diagn Ther , vol.11 , pp. 335-340
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  • 8
    • 0018305302 scopus 로고
    • A new lethal syndrome with cloudy corneae, diaphragmatic defects and distal limb deformities
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    • (1979) Hum Genet , vol.50 , pp. 65-70
    • Fryns, J.P.1    Moerman, F.2    Goddeeris, P.3    Bossuyt, C.4    Van den Berghe, H.5
  • 9
    • 0034605366 scopus 로고    scopus 로고
    • Discordant phenotype in monozygotic twins with Fryns syndrome
    • Vargas JE, Cox GF, Korf BR. Discordant phenotype in monozygotic twins with Fryns syndrome. Am J Med Genet 2000;94:42-45.
    • (2000) Am J Med Genet , vol.94 , pp. 42-45
    • Vargas, J.E.1    Cox, G.F.2    Korf, B.R.3
  • 10
    • 0028789524 scopus 로고
    • Fryns syndrome: Two further cases without lateral diaphragmatic defects
    • Bartsch O, Meinecke P, Kamin G. Fryns syndrome: two further cases without lateral diaphragmatic defects. Clin Dysmorphol 1995;4:352-358.
    • (1995) Clin Dysmorphol , vol.4 , pp. 352-358
    • Bartsch, O.1    Meinecke, P.2    Kamin, G.3
  • 11
    • 0031748601 scopus 로고    scopus 로고
    • Scalp defects in Fryns syndrome
    • Fryns JP. Scalp defects in Fryns syndrome. Genet Couns 1998;9:153-154.
    • (1998) Genet Couns , vol.9 , pp. 153-154
    • Fryns, J.P.1
  • 15
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    • Hematometra and sudden death after status epilepticus in the adolescent female with Fryns syndrome
    • Dingens M, Fryns JP. Hematometra and sudden death after status epilepticus in the adolescent female with Fryns syndrome. Genet Couns 1999;10:329-330.
    • (1999) Genet Couns , vol.10 , pp. 329-330
    • Dingens, M.1    Fryns, J.P.2
  • 16
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    • Fryns syndrome: A rare familial cause of congenital diaphragmatic hernia
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    • (1994) J Pediatr Surg , vol.29 , pp. 1266-1267
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.