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2001, Number 4

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Rev Fac Med UNAM 2001; 44 (4)

Congenital anomalies with multiple spleens

Durán PMA, Guereña EA
Full text How to cite this article

Language: Spanish
References: 16
Page: 185-187
PDF size: 60.58 Kb.


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REFERENCES

  1. Winer-Muram HT. Adult presentation of heterotaxic syndromes and related complexes. J Thorac Imaging 1995; 10: 43-57.

  2. Kenneth LJ. Smith‘s recognizable patterns of human malformation 5ª. Ed WB Saunders Company 1997.

  3. Applegate KE, Goske MJ, Pierce G, Murphy D. Situs revisited: imaging of the heterotaxy syndrome. Radiographics 1999; 19: 837-52.

  4. Britz-Cunningham SH, Shah MM, Zuppan CW, Fletcher WH. Mutations of the connexin 43 Gap-junction gene in patients with heart malformations and defects of laterality. New Engl J Med 1995; 332: 1323-9.

  5. 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.

  6. Mikkila SP, Janas M, Karikoski R, Tarkkila T, Simola KOJ. X-linked laterality sequence in a family with carrier manifestations. Am J Med Genet 1994; 49: 35-438.

  7. Casey B, Cuneo BF, Vitali C, Van Hecke H, Barrish J, Hicks J et al. Ballabio A, Hoo JJ, Autosomal dominant transmission of familial laterality defects. Am J Med Genet 1996; 61: 325-328.

  8. Mc Chane RH, Heisch JH, Russel LJ, Weisskopf B. Ivemark‘s “asplenia” syndrome: a single gene disorder. South Med J 1989; 82: 1312-3.

  9. Carmi R, Boughman JA, Rosembaum KR. Human situs determination is probably controlled by several different genes. Am J Med Genet 1992; 44: 246-9.

  10. Walman JD, Rosenthal A, Smith AL, Shurins S, Nadas AS. Sepsis and congenitalasplenia. J Pediatr.

  11. Gilbert-Barnes E. Respiratory system: Gilbert-Barnes E. Potter‘s Pathology of the fetus and infant Vol 1, Mosby-Year Book, Inc. 1997. P728.

  12. Layman TE, Levine MA, Amplatz K et al. Asplenic syndrome in association with rudimentary spleen. Am J Cardiol 1968; 20: 136.

  13. Sánchez J, Villavicencio R, Domingo J, Martínez PA. “Ivemark`s syndrome” with a normally developed spleen. Arch Inst Cardiol Mex 1973; 43: 325-329.

  14. Epstein ML, Formanek AG, Bessinger FB, Edwards JE. Clinical pathological conference. Am Heart 1980; 99: 510-516.

  15. Distefano G, Romeo MG, Grasso S, Mazzone D, Sciacca P, Mollica F. Dextrocardia with and without situs fiscerum inversus in two sibs. Am J Med Genet 1987; 27: 929-934.

  16. Moerman P, Verbeken E, Fryns JP, Goddeeris P, Lauweryns JM. Associations of Meckel syndrome with M-anisosplenia in one patient. Clin Genet 1982; 22: 143-147.




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Rev Fac Med UNAM . 2001;44