메뉴 건너뛰기




Volumn 23, Issue 4, 2004, Pages 561-564

Antenatal Sonographic Features of Perlman Syndrome

Author keywords

[No Author keywords available]

Indexed keywords

DISEASES; GROWTH KINETICS; ULTRASONIC EFFECTS;

EID: 2442564627     PISSN: 02784297     EISSN: None     Source Type: Journal    
DOI: 10.7863/jum.2004.23.4.561     Document Type: Article
Times cited : (8)

References (18)
  • 1
    • 0014772767 scopus 로고
    • Metanephric hamartomas and nephroblastomatosis in siblings
    • Liban E, Kozenitzky IL. Metanephric hamartomas and nephroblastomatosis in siblings. Cancer 1970; 25:885-888.
    • (1970) Cancer , vol.25 , pp. 885-888
    • Liban, E.1    Kozenitzky, I.L.2
  • 2
    • 0015781893 scopus 로고
    • Renal hamartomas and nephroblastomatosis with fetal gigantism: A familial syndrome
    • Perlman M, Goldberg GM, Bar-Ziv J, Danovitch G. Renal hamartomas and nephroblastomatosis with fetal gigantism: a familial syndrome. J Pediatr 1973; 83:414-418.
    • (1973) J Pediatr , vol.83 , pp. 414-418
    • Perlman, M.1    Goldberg, G.M.2    Bar-Ziv, J.3    Danovitch, G.4
  • 3
    • 0016794720 scopus 로고
    • Syndrome of fetal gigantism, renal hamartomas, and nephroblastomatosis with Wilms' tumor
    • Perlman M, Levin M, Wittels B. Syndrome of fetal gigantism, renal hamartomas, and nephroblastomatosis with Wilms' tumor. Cancer 1975; 35:1212-1217.
    • (1975) Cancer , vol.35 , pp. 1212-1217
    • Perlman, M.1    Levin, M.2    Wittels, B.3
  • 4
    • 0023017259 scopus 로고
    • Perlman syndrome: Familial renal dysplasia with Wilms tumor, fetal gigantism, and multiple congenital anomalies [letter]
    • Perlman M. Perlman syndrome: familial renal dysplasia with Wilms tumor, fetal gigantism, and multiple congenital anomalies [letter]. Am J Med Genet 1986; 25:793-795.
    • (1986) Am J Med Genet , vol.25 , pp. 793-795
    • Perlman, M.1
  • 5
    • 0021229493 scopus 로고
    • The Perlman syndrome: Familial renal dysplasia with Wilms tumor, fetal gigantism and multiple congenital anomalies
    • Neri G, Martini-Neri ME, Katz BE, Opitz JM. The Perlman syndrome: familial renal dysplasia with Wilms tumor, fetal gigantism and multiple congenital anomalies. Am J Med Genet 1984; 19:195-207.
    • (1984) Am J Med Genet , vol.19 , pp. 195-207
    • Neri, G.1    Martini-Neri, M.E.2    Katz, B.E.3    Opitz, J.M.4
  • 6
    • 0031891797 scopus 로고    scopus 로고
    • Perlman syndrome: A case report emphasizing its similarity to and distinction from Beckwith-Wiedemann and prune-belly syndromes
    • Fahmy J, Kaminsky CK, Parisi MT. Perlman syndrome: a case report emphasizing its similarity to and distinction from Beckwith-Wiedemann and prune-belly syndromes. Pediatr Radiol 1998; 28: 179-182.
    • (1998) Pediatr Radiol , vol.28 , pp. 179-182
    • Fahmy, J.1    Kaminsky, C.K.2    Parisi, M.T.3
  • 7
    • 0031896606 scopus 로고    scopus 로고
    • Prenatal ultrasound observations in subsequent pregnancies with Perlman syndrome
    • van der Stege JG, van Eyck J, Arabin B. Prenatal ultrasound observations in subsequent pregnancies with Perlman syndrome. Ultrasound Obstet Gynecol 1998; 11:149-151.
    • (1998) Ultrasound Obstet Gynecol , vol.11 , pp. 149-151
    • Van Der Stege, J.G.1    Van Eyck, J.2    Arabin, B.3
  • 9
    • 0031761779 scopus 로고    scopus 로고
    • Perlman syndrome: A cause of enlarged, hyperechogenic kidneys
    • Chitty LS, Clark T, Maxwell D. Perlman syndrome: a cause of enlarged, hyperechogenic kidneys. Prenat Diagn 1998; 18:1163-1168.
    • (1998) Prenat Diagn , vol.18 , pp. 1163-1168
    • Chitty, L.S.1    Clark, T.2    Maxwell, D.3
  • 10
    • 0030950727 scopus 로고    scopus 로고
    • Extending the overlap of three congenital overgrowth syndromes
    • Coppin B, Moore I, Hatchwell E. Extending the overlap of three congenital overgrowth syndromes. Clin Genet 1997; 51:375-378.
    • (1997) Clin Genet , vol.51 , pp. 375-378
    • Coppin, B.1    Moore, I.2    Hatchwell, E.3
  • 11
    • 0026483207 scopus 로고
    • Perlman and Wiedemann-Beckwith syndromes: Two distinct conditions associated with Wilms' tumour
    • Grundy RG, Pritchard J, Baraitser M, Risdon A, Robards M. Perlman and Wiedemann-Beckwith syndromes: two distinct conditions associated with Wilms' tumour. Eur J Pediatr 1992; 151:895-898.
    • (1992) Eur J Pediatr , vol.151 , pp. 895-898
    • Grundy, R.G.1    Pritchard, J.2    Baraitser, M.3    Risdon, A.4    Robards, M.5
  • 12
    • 0022486675 scopus 로고
    • The Perlman familial nephroblastomatosis syndrome
    • Greenberg F, Stein F, Gresik MV, et al. The Perlman familial nephroblastomatosis syndrome. Am J Med Genet 1986; 24:101-110.
    • (1986) Am J Med Genet , vol.24 , pp. 101-110
    • Greenberg, F.1    Stein, F.2    Gresik, M.V.3
  • 13
    • 0342902019 scopus 로고
    • A case of Perlman syndrome associated with a cytogenetic abnormality of chromosome 11
    • Chernos JE, Fowler SB, Cox DM. A case of Perlman syndrome associated with a cytogenetic abnormality of chromosome 11 [abstract]. Am J Hum Genet 1990; 47(suppl):A28.
    • (1990) Am J Hum Genet , vol.47 , Issue.SUPPL.
    • Chernos, J.E.1    Fowler, S.B.2    Cox, D.M.3
  • 14
    • 0034006094 scopus 로고    scopus 로고
    • A case of Perlman syndrome: Fetal gigantism, renal dysplasia, and severe neurological deficits
    • Schilke K, Schaefer F, Waldherr R, et al. A case of Perlman syndrome: fetal gigantism, renal dysplasia, and severe neurological deficits. Am J Med Genet 2000; 91:29-33.
    • (2000) Am J Med Genet , vol.91 , pp. 29-33
    • Schilke, K.1    Schaefer, F.2    Waldherr, R.3
  • 15
    • 0023193362 scopus 로고
    • Genetic mechanisms of tumor-specific loss of 11p DNA sequences in Wilms tumor
    • Dao DD, Schroeder WT, Chao LY, et al. Genetic mechanisms of tumor-specific loss of 11p DNA sequences in Wilms tumor. Am J Hum Genet 1987; 41:202-217.
    • (1987) Am J Hum Genet , vol.41 , pp. 202-217
    • Dao, D.D.1    Schroeder, W.T.2    Chao, L.Y.3
  • 16
    • 0029848437 scopus 로고    scopus 로고
    • Molecular biology of Beckwith-Wiedemann syndrome
    • Weksberg R, Squire JA. Molecular biology of Beckwith-Wiedemann syndrome. Med Pediatr Oncol 1996; 27:462-469.
    • (1996) Med Pediatr Oncol , vol.27 , pp. 462-469
    • Weksberg, R.1    Squire, J.A.2
  • 17
    • 0025362975 scopus 로고
    • Loss of heterozygosity in Wilms' tumors, studied for 6 putative tumor suppressor regions, is limited to chromosome 11
    • Mannens M, Devilee P, Bliek J, et al. Loss of heterozygosity in Wilms' tumors, studied for 6 putative tumor suppressor regions, is limited to chromosome 11. Cancer Res 1990; 50:3279-3283.
    • (1990) Cancer Res , vol.50 , pp. 3279-3283
    • Mannens, M.1    Devilee, P.2    Bliek, J.3
  • 18


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.