儿童肾母细胞瘤并11号环状染色体1例报道

张昊,冯晨,唐锁勤

中国当代儿科杂志 ›› 2012, Vol. 14 ›› Issue (12) : 993-994.

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中国当代儿科杂志 ›› 2012, Vol. 14 ›› Issue (12) : 993-994.
病例报告

儿童肾母细胞瘤并11号环状染色体1例报道

  • 张昊,冯晨,唐锁勤
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Wilms' tumor and ring chromosome 11 in a child

  • ZHANG Hao, FENG Chen, TANG Suo-Qin
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张昊,冯晨,唐锁勤. 儿童肾母细胞瘤并11号环状染色体1例报道[J]. 中国当代儿科杂志. 2012, 14(12): 993-994
ZHANG Hao, FENG Chen, TANG Suo-Qin. Wilms' tumor and ring chromosome 11 in a child[J]. Chinese Journal of Contemporary Pediatrics. 2012, 14(12): 993-994
中图分类号: R596.1   

参考文献

[1]Rivera MN, Haber DA. Wilms' tumour: connecting tumorigenesis and organ development in the kidney[J]. Nat Rev Cancer, 2005, 5(9): 699-712.

[2]Romain DR, Gebbie OB, Parfitt RG, Columbano-Green LM, Smythe RH, Chapman CJ, et al. Two cases of ring chromosome 11[J]. J Med Genet, 1983, 20(5): 380-382.

[3]Cousineau AJ, Higgins JV, Scott-Emuakpor AB, Mody G. Brief clinical report: ring-11 chromosome: Phenotype-karyotype correlation with deletions of 11q[J]. Am J Med Genet, 1983, 14(1): 29-35.

[4]Bedoyan JK, Flore LA, Alkatib A, Ebrahim SA, Bawle EV. Transmission of ring chromosome 13 from a mother to daughter with both having a 46, XX, r(13)(p13q34) karyotype[J]. Am J Med Genet A, 2004, 129A(3): 316-320.

[5]王金根,高解春. 肾母细胞瘤[M]//高解春,王耀平. 现代小儿肿瘤学.上海:复旦大学出版社,2003:519-537.

[6]D'Angio GJ. The national Wilm's Tumor Study: a 40 year perspective[J]. Lifetime Data Anal, 2007, 13(4): 463-470.

[7]Sanker VH, Phadke SR. Ring chromosome 13 in an infant with ambiguous genitalia[J]. Indian Pediatr, 2006, 43(3): 258-260.

[8]Rivera MN. Haber DA. Wilm's tumour: connecting tumorigenesis and organ development in the kidney[J]. Nat Rev Cancer, 2005, 5(9): 699-712.

[9]陆颖,朱茂祥.人类11号染色体与肿瘤[J].国外医学·生理病理科学与临床分册,2002,22(4):362-365.

[10]Amor DJ, Voullaire L, Bentley K, Savarirayan R, Choo KH. Mosaic monosomy of a neocentric ring chromosome maps brachyphalangy and growth hormone deficiency to 13q31-1-13q32-3 [J]. Am J Med Genet A, 2005, 133A (2): 151-157.

[11]Gentile M, Buonadonna AL, Cariola F, Fiorente P, Valenzano MC, Guanti G. Molecular and cytogenetic characterization of an unusual case of partial trisomy/Partial monosomy 13 mosaicism: 46, XX, r(13) (p11q14)/46, XX, der(13) t(13; 13)(q10; q14.) [J]. J Med Genet, 1999, 36(1): 77-82.

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