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Volumn 51, Issue 3, 1997, Pages 200-204

Clinical manifestation of a severe neonatal progeroid syndrome

Author keywords

Cutis laxa; De Barsy; Hallermann Streiff; Mandibuloacral dysplasia; Neonatal progeria; Wiedmann Rautenstrauch

Indexed keywords

ARTHROGRYPOSIS; ARTICLE; BLEPHAROPHIMOSIS; CASE REPORT; CATARACT; CLINICAL FEATURE; CUTIS LAXA; FEMALE; HALLERMANN STREIFF SYNDROME; HUMAN; NEWBORN; PRIORITY JOURNAL; PROGERIA; PULMONARY VALVE STENOSIS;

EID: 1842370240     PISSN: 00099163     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1399-0004.1997.tb02453.x     Document Type: Article
Times cited : (11)

References (15)
  • 1
    • 0024249145 scopus 로고
    • New syndromes. Part II: European syndromes
    • Beemer FA. New syndromes. Part II: European syndromes. Am J Med Genet 1988: Suppl 4: 71-84.
    • (1988) Am J Med Genet , vol.4 , Issue.SUPPL. , pp. 71-84
    • Beemer, F.A.1
  • 2
    • 0029039759 scopus 로고
    • The Wiedmann-Rautenstrauch neonatal progeroid syndrome: A case report and review of the literature
    • Bitoun P, Lachassine E, Sellier N, Sauvion S, Gaudelus J. The Wiedmann-Rautenstrauch neonatal progeroid syndrome: a case report and review of the literature. Clin Dysmorphol 1995: 4: 239-245.
    • (1995) Clin Dysmorphol , vol.4 , pp. 239-245
    • Bitoun, P.1    Lachassine, E.2    Sellier, N.3    Sauvion, S.4    Gaudelus, J.5
  • 3
    • 0025786734 scopus 로고
    • Hallermann-Streiff syndrome: A review
    • Cohen Jr Michael M. Hallermann-Streiff syndrome: a review. Am J Med Genet 1991: 41: 488-499.
    • (1991) Am J Med Genet , vol.41 , pp. 488-499
    • Cohen Jr., M.M.1
  • 4
    • 0014293393 scopus 로고
    • Dwarfism, oligophrenia and degeneration of the elastic tissue in skin and cornea. A new syndrome?
    • De Barsy AM, Moens E, Dierckx L. Dwarfism, oligophrenia and degeneration of the elastic tissue in skin and cornea. A new syndrome? Helv Paediatr Acta 1968: 3: 305-313.
    • (1968) Helv Paediatr Acta , vol.3 , pp. 305-313
    • De Barsy, A.M.1    Moens, E.2    Dierckx, L.3
  • 5
    • 0019464952 scopus 로고
    • The Wiedmann-Rautenstrauch or neonatal progeroid syndrome. Report of a patient with consanguineous parents
    • Devos EA, Leroy JG, Frijns JP, Van den Berghe H. The Wiedmann-Rautenstrauch or neonatal progeroid syndrome. Report of a patient with consanguineous parents. Eur J Pediatr 1981: 136: 245-248.
    • (1981) Eur J Pediatr , vol.136 , pp. 245-248
    • Devos, E.A.1    Leroy, J.G.2    Frijns, J.P.3    Van den Berghe, H.4
  • 7
    • 0015134828 scopus 로고
    • Congenital athetosis, mental deficiency, dwarfism and laxity of skin and ligaments
    • Hoefnagel D, Pomeroy J, Wurster D, Saxon A. Congenital athetosis, mental deficiency, dwarfism and laxity of skin and ligaments. Helv Paediat Acta 1971: 26: 397-402.
    • (1971) Helv Paediat Acta , vol.26 , pp. 397-402
    • Hoefnagel, D.1    Pomeroy, J.2    Wurster, D.3    Saxon, A.4
  • 8
    • 0026569289 scopus 로고
    • De Barsy syndrome: Report of a case, literature review, and elastin gene expression studies of the skin
    • Karnes PS, Shamban AT, Olsen DR, Fazio MJ, Falk RE. De Barsy syndrome: report of a case, literature review, and elastin gene expression studies of the skin. Am J Med Genet 1992: 42: 29-34.
    • (1992) Am J Med Genet , vol.42 , pp. 29-34
    • Karnes, P.S.1    Shamban, A.T.2    Olsen, D.R.3    Fazio, M.J.4    Falk, R.E.5
  • 11
    • 0023620984 scopus 로고
    • Neonatal progeroid syndrome: Report of a Japanese infant
    • Ohashi H, Eguchi T, Kajii T. Neonatal progeroid syndrome: report of a Japanese infant. Jpn J Hum Genet 1987: 32: 253-256.
    • (1987) Jpn J Hum Genet , vol.32 , pp. 253-256
    • Ohashi, H.1    Eguchi, T.2    Kajii, T.3
  • 12
    • 0023932602 scopus 로고
    • The neonatal pseudo-hydrocephalic progeroid syndrome (Wiedmann-Rautenstrauch). Report of a new patient and review of the literature
    • Rudin C, Thommen L, Fliegel C, Steinmann B, Buhler U. The neonatal pseudo-hydrocephalic progeroid syndrome (Wiedmann-Rautenstrauch). Report of a new patient and review of the literature. Eur J Pediatr 1988: 147: 433-438.
    • (1988) Eur J Pediatr , vol.147 , pp. 433-438
    • Rudin, C.1    Thommen, L.2    Fliegel, C.3    Steinmann, B.4    Buhler, U.5
  • 14
    • 0025216463 scopus 로고
    • Wiedmann-Rautenstrauch syndrome
    • Toriello HV. Wiedmann-Rautenstrauch syndrome. J Med Genet 1990: 27: 256-257.
    • (1990) J Med Genet , vol.27 , pp. 256-257
    • Toriello, H.V.1
  • 15
    • 0018373151 scopus 로고
    • An unidentified neonatal progeroid syndrome: Follow-up report
    • Wiedmann HR. An unidentified neonatal progeroid syndrome: follow-up report. Eur J Pediatr 1979: 130: 65-70.
    • (1979) Eur J Pediatr , vol.130 , pp. 65-70
    • Wiedmann, H.R.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.