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Pediatric Pathology & Molecular Medicine Volume 21, 2002 - Issue 5
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Research Article

SEQUENCE OF RIGHT LATERALITY WITH SPLEEN: WIDENING THE SPECTRUM OF HETEROTAXY

Marco A. Durán Unidad de Patología del Hospital General de México y Facultad de Medicina de la UNAMCorrespondence[email protected]
&
Avril Guereña Unidad de Patología del Hospital General de México y Facultad de Medicina de la UNAM
Pages 461-465 | Published online: 09 Jul 2009

  • Winer - Muram HT. Adult presentation of heterotaxic syndromes and related complexes. J. Thorac Imaging 1995;10:43-57.
  • Kenneth LJ. Smith's recognizable patterns of human malformation. 5th ed. Philadelphia: WB Saunders, 1997.
  • Applegate KE, Goske MJ, Pierce G, Murphy D. Situs revisited: Imaging of the heterotaxy syndrome. Radiographies 1999;19:387-452.
  • Britz - Cunningham SH, Shan MM, Zuppan CW, Fletcher WH. Mutations of the connexin 43 Gap - junction gene in patients with heart malformations and defects of laterality. New Eng J Med 1995;332:1323-1329.
  • Casey B, Devoto M, Jones KL, Ballabio A. Mapping a gene for familial situs abnormalities to human chromosome Xq24 - q27.1. Nature Genet 1993;5:403-407.
  • Mikkila SP, Janas M, Karikoski R, Tarkkila T, Simola KOJ. X - linked laterality sequence in family with carrier manifestations. Am J Med Genet 1994;49:435-438.
  • Casey B, Cuneo BF, Vitali C, Van Hecke H, Barrish J, Hicks J, et al. Autosomal dominant transmission of family laterality defects, Am J Med Genet 1996;61:325-328.
  • McChane RH, Heisch JH, Russell LJ, Weisskopf B. Ivemark's "asplenia" syndrome: A single gene disorder. South Med J 1989;82:1312-1313.
  • Carmi R, Boughman JA, Rosembaum KR. Human situs determination is probably controled by several different genes. Am J Med Genet 1992;44:246-249.
  • Waldman JD, Rosenthal A, Smith AL, Shurins S, Nadas AS. Sepsis and congenital asplenia. J Pediatr 1977;90:555-559.
  • Gilbert - Barnes E. Respiratory system. In Gilbert Barnes E, ed. Potter's Pathology of the fetus and infant, vol 1. St. Louis, MO: Mosby - Year Book, Inc., 1997:728.
  • LaymanTE, Levine MA, Amplatz K, et al. Asplenic syndrome in association with rudimentary spleen. Am J Cardiol 1968;20:!36.
  • Sanchez J, Villavicencio R, Domingo J, Martinez PA. "Ivemark's syndrome" with a normally developed spleen. Arch Inst Cardiol Mex 1973;43:325-329.
  • Epstein ML, Formanek AG, Bessinger FB, Edwards JE. Clinical pathological conference. Am Heart J 1980;99:510-516.
  • Distefano G, Romeo MG, Grasso S, Mazzone D, Sciacca P, Mollica F. Dextrocardia with and without situs viscerum inversus in two sibs. Am J Med Genet 1987;27:929-934.
  • Moerman P, Verbcken E, Fryns JP, Goddeeris P, Lauweryns JM. Association of Meckel syndromewith M - anisosplenia in one patient. Clin Genet 1982;22:147-147.

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