Heyeditary spherocytosis in neonatal period: a case report and literature review
Keywords:
jaundice, neonatal, spherocytosis, hereditary, infant, newbornAbstract
A clinical case of hereditary spherocytosis in neonatal
period as well as a literature review are reported. Clinical, laboratorial, evolutive and therapeutic aspects are discussed. The importance of differential diagnosis with ABO incompatibihty hemolytic disease is emphasized
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GALLAGHER, P.G., TSE, W.T., FORGET, B.G. Clinical and molecular aspects of disorders ofthe erythrocyte membrane skeleton. Seminars in Perinatology , Philadelphia, v.14, p.351-367, 1990,
IOLASCON,A., DELGIUDICE, E.M., CAMASCHELLA C. Molecular pathology of inherited erythocyte membrane disordes: hereditary spherocytosis and elliptocytosis. Haemalologtca, v.77, p.60-72, Jan/Feb. 1992.
KOSTINAS, J.E., CANTOW, E.F., WETZEL, R.A. Autohemolysis of cord blood in congenital spherocytosis and ABO incompatibility. Journal of Pediatrics. St. Louis, v.70, n.2, p.273-276, 1967.
KRUEGER, H,C., BURGERT JR., E.O. Hereditary spherocytosis in 100 childreen. Mayo Clinic Proceedings, Rochester, v.41, n.12, p.821-830, 1966.
LUX, S.E. Disorders of the red all membrane. In NATHAN, D. G., OSKI, E. A. (Ed.). Hematology of infancy and childhood. 3.ed. Philadelphia: W.B. Saunders, 1988. p.443-544.
MORTON, N. E., MAC KINNEY, A. A., KOSOWER, N. S., SCHILLING, R. F., GRAY, M. P. Genetics of spherocytosis. American Journal of Human Genetics , Chicago, v.14, p. 170- 184, 1962.
OSKI, F. A., NAIMAN, J. L. Hematologia do RN. 3.ed. São Paulo : Manole, 1984. 380p
STEVENS, R. F., EVANS, D. I. K. Congenital spherocytosis is often not hereditary. Clinical Pediatrics, Philadelphia, v.20, n. 1, p.47-49, 1981.
THURMAN, W. G. Changes in red cell fragility with infection. American Journal of Diseases of Children, Chicago, v.100, p.639, 1960.
TRUCCO, J.I.. BROWN, A.K. Neonatal manifestations of hereditary spherocytosis. American Journal of Diseases of Children, Chicago, v. 113, p.263-270, Feb. 1967
WONG, W. Y., POWARS, D. R., ABDALLA, C. Phototerapy failure in jaundiced newborns with hereditary spherocytosis. Acta Paediatrica Scandinavica. Oslo, v.79, p.368-369, Mar. 1990.
YOUNG, L. E. Hereditary spherocytosis. American Journal of Medicine, Newton, v.28, p.486-497, Mar. 1955.
. ZIPURSKY, A.. CHINTN, C., BROWN. E.. BROWN, E. J. The quantification of spherocytes in ABO hemolytic disease. Journal of Pediatrics, St. Louis, v.94, n.6, p.965-967, 1979