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Volumn 16, Issue 1-2, 2000, Pages 134-135

A case of Currarino triad with familial sacral bony deformities

Author keywords

Currarino triad; Familial occurrence; Sacral bony deformity

Indexed keywords

ARTICLE; BONE MALFORMATION; BONE RADIOGRAPHY; CASE REPORT; CHROMOSOME ANALYSIS; CURRARINO TRIAD; FAMILIAL DISEASE; HUMAN; MALE; NEWBORN; PRIORITY JOURNAL; RECTUM FISTULA; SACROCOCCYX TERATOMA; SCREENING; URETHRA FISTULA;

EID: 0034066497     PISSN: 01790358     EISSN: None     Source Type: Journal    
DOI: 10.1007/s003830050042     Document Type: Article
Times cited : (25)

References (4)
  • 1
    • 0019870232 scopus 로고
    • Triad of anorectal, sacral, and presacral anomalies
    • Currarino G, Colon D, Votteler T (1981) Triad of anorectal, sacral, and presacral anomalies. A J R 137: 395-398
    • (1981) A J R , vol.137 , pp. 395-398
    • Currarino, G.1    Colon, D.2    Votteler, T.3
  • 2
    • 0029905695 scopus 로고    scopus 로고
    • The Currarino syndrome -hereditary transmitted syndrome of anorectal, sacral and presacral anomalies. Case report and review of the literature
    • Kochling J, Pistor G, Marzhauser Brands S, et al (1996) The Currarino syndrome -hereditary transmitted syndrome of anorectal, sacral and presacral anomalies. Case report and review of the literature. Eur J Pediatr Surg 6: 114-119
    • (1996) Eur J Pediatr Surg , vol.6 , pp. 114-119
    • Kochling, J.1    Pistor, G.2    Marzhauser Brands, S.3
  • 3
    • 0031025160 scopus 로고    scopus 로고
    • Currarino triad: Anorectal malformation, sacral bony abnormality, and presacral mass - A review of 11 cases
    • Lee SC, Chun YS, Jung SE, et al (1997) Currarino triad: anorectal malformation, sacral bony abnormality, and presacral mass - a review of 11 cases. J Pediatr Surg 32: 58-61
    • (1997) J Pediatr Surg , vol.32 , pp. 58-61
    • Lee, S.C.1    Chun, Y.S.2    Jung, S.E.3
  • 4
    • 0029909850 scopus 로고    scopus 로고
    • Currarino triad with a terminal deletion 7q35-qter
    • Masuo M, Imaizumi K, Aida N, et al (1996) Currarino triad with a terminal deletion 7q35-qter. J Med Genet 33: 877-878
    • (1996) J Med Genet , vol.33 , pp. 877-878
    • Masuo, M.1    Imaizumi, K.2    Aida, N.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.