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Volumn 114, Issue 2, 2007, Pages 270-271

A case of PAGOD syndrome with hypoplastic left heart syndrome

Author keywords

[No Author keywords available]

Indexed keywords

ANASTOMOSIS; ARTICLE; CASE REPORT; CLINICAL FEATURE; DIAPHRAGM EVENTRATION; FONTAN PROCEDURE; GONADAL AGENESIS; HORSESHOE LUNG; HUMAN; HYPOPLASTIC LEFT HEART SYNDROME; KARYOTYPE 46,XY; LUNG HYPOPLASIA; LUNG MALFORMATION; MALFORMATION SYNDROME; MITRAL VALVE ATRESIA; NORWOOD PROCEDURE; PAGOD SYNDROME; PRESCHOOL CHILD; PRIORITY JOURNAL; SCIMITAR SYNDROME; TREATMENT OUTCOME;

EID: 33751229600     PISSN: 01675273     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ijcard.2005.11.068     Document Type: Article
Times cited : (25)

References (6)
  • 1
    • 0025840371 scopus 로고
    • Double vagina, cardiac, pulmonary, and other genital malformations with 46,XY karyotype
    • Meacham L.R., Winn K.J., Culler F.L., and Parks J.S. Double vagina, cardiac, pulmonary, and other genital malformations with 46,XY karyotype. Am J Med Genet 41 (1991) 478-481
    • (1991) Am J Med Genet , vol.41 , pp. 478-481
    • Meacham, L.R.1    Winn, K.J.2    Culler, F.L.3    Parks, J.S.4
  • 2
    • 0027445096 scopus 로고
    • Familial occurrence of agonadism and multiple internal malformations in phenotypically normal girls with 46,XY and 46,XX karyotypes, respectively: a new autosomal recessive syndrome
    • Kennerknecht I., Sorgo W., Oberhoffer R., et al. Familial occurrence of agonadism and multiple internal malformations in phenotypically normal girls with 46,XY and 46,XX karyotypes, respectively: a new autosomal recessive syndrome. Am J Med Genet 47 (1993) 1166-1170
    • (1993) Am J Med Genet , vol.47 , pp. 1166-1170
    • Kennerknecht, I.1    Sorgo, W.2    Oberhoffer, R.3
  • 3
    • 0025998375 scopus 로고
    • Gonadal agenesis in a 46,XY female with multiple malformations and positive testing for the sex-determining region of the Y chromosome
    • Sorgo W., Gortner L., Bartmann P., et al. Gonadal agenesis in a 46,XY female with multiple malformations and positive testing for the sex-determining region of the Y chromosome. Horm Res 35 (1991) 124-131
    • (1991) Horm Res , vol.35 , pp. 124-131
    • Sorgo, W.1    Gortner, L.2    Bartmann, P.3
  • 4
    • 0026509497 scopus 로고
    • Phenotypically normal girl with male pseudohermaphroditism, hypoplastic left ventricle, lung aplasia, horseshoe kidney, and diaphragmatic hernia
    • Maaswinkel-Mooij P.D., and Stokvis-Brantsma W.H. Phenotypically normal girl with male pseudohermaphroditism, hypoplastic left ventricle, lung aplasia, horseshoe kidney, and diaphragmatic hernia. Am J Med Genet 42 (1992) 647-648
    • (1992) Am J Med Genet , vol.42 , pp. 647-648
    • Maaswinkel-Mooij, P.D.1    Stokvis-Brantsma, W.H.2
  • 5
    • 0034054304 scopus 로고    scopus 로고
    • Sex reversal and diaphragmatic hernia in phenotypically female sibs with normal XY chromosomes
    • Manouvrier-Hanu S., Besson R., Cousin L., et al. Sex reversal and diaphragmatic hernia in phenotypically female sibs with normal XY chromosomes. J Med Genet 37 (2000) 315-318
    • (2000) J Med Genet , vol.37 , pp. 315-318
    • Manouvrier-Hanu, S.1    Besson, R.2    Cousin, L.3
  • 6
    • 0037087345 scopus 로고    scopus 로고
    • PAGOD syndrome: eighth case and comparison to animal models of congenital vitamin A deficiency
    • Macayran J.F., Doroshow R.W., Phillips J., et al. PAGOD syndrome: eighth case and comparison to animal models of congenital vitamin A deficiency. Am J Med Genet 108 (2002) 229-234
    • (2002) Am J Med Genet , vol.108 , pp. 229-234
    • Macayran, J.F.1    Doroshow, R.W.2    Phillips, J.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.