메뉴 건너뛰기




Volumn 27, Issue 4, 2007, Pages 252-254

Nonimmune hydrops fetalis in two cases of consanguineous parents and associated with hereditary spherocytosis and hemophagocytic hystiocytosis

Author keywords

[No Author keywords available]

Indexed keywords

ALANINE AMINOTRANSFERASE; ALBUMIN; ALKALINE PHOSPHATASE; ASPARTATE AMINOTRANSFERASE; BILIRUBIN; FERRITIN; FIBRINOGEN; FOLIC ACID; FRESH FROZEN PLASMA; GRANULOCYTE COLONY STIMULATING FACTOR; HEMOGLOBIN; TRIACYLGLYCEROL;

EID: 33947709395     PISSN: 07438346     EISSN: 14765543     Source Type: Journal    
DOI: 10.1038/sj.jp.7211657     Document Type: Article
Times cited : (15)

References (17)
  • 1
    • 0023019267 scopus 로고
    • Nonimmune hydrops fetalis: Clinical experience and factors related to a poor outcome
    • Castillo RA, Devoe LD, Hadi HA, Martin S, Geist D. Nonimmune hydrops fetalis: Clinical experience and factors related to a poor outcome. Am J Obstet Gynecol 1986; 155: 812-816.
    • (1986) Am J Obstet Gynecol , vol.155 , pp. 812-816
    • Castillo, R.A.1    Devoe, L.D.2    Hadi, H.A.3    Martin, S.4    Geist, D.5
  • 2
    • 0029610176 scopus 로고
    • Non immune fetal hydrops: Diagnosis and obstetrical management
    • Jones DC. Non immune fetal hydrops: Diagnosis and obstetrical management. Semin Perinatol 1995; 19: 447-461.
    • (1995) Semin Perinatol , vol.19 , pp. 447-461
    • Jones, D.C.1
  • 3
    • 0025719950 scopus 로고
    • Deficiency of α-spectrin synthesis in burst forming units - Erythroid in lethal hereditary spherocytosis
    • Whitfield CF, Follweiler JB, Morrow LL, Miller BA. Deficiency of α-spectrin synthesis in burst forming units - erythroid in lethal hereditary spherocytosis. Blood 1991; 78: 3043-3051.
    • (1991) Blood , vol.78 , pp. 3043-3051
    • Whitfield, C.F.1    Follweiler, J.B.2    Morrow, L.L.3    Miller, B.A.4
  • 4
    • 0031017565 scopus 로고    scopus 로고
    • Mutation of a highly conserved residue of betaI spectrin associated with fatal and near-fatal neonatal hemolytic anemia
    • Gallagher PG, Petruzzi MJ, Weed SA, Zhang Z, Marchesi SL, Mohandas N et al. Mutation of a highly conserved residue of betaI spectrin associated with fatal and near-fatal neonatal hemolytic anemia. J Clin Invest 1997; 99: 267-277.
    • (1997) J Clin Invest , vol.99 , pp. 267-277
    • Gallagher, P.G.1    Petruzzi, M.J.2    Weed, S.A.3    Zhang, Z.4    Marchesi, S.L.5    Mohandas, N.6
  • 5
    • 0028927524 scopus 로고
    • Recurrent fatal hydrops fetalis associated with a nucleotide substitution in the erythrocyte beta-spectrin gene
    • Gallagher PG, Weed SA, Tse WT, Benoit L, Morrow JS, Marchesi SL et al. Recurrent fatal hydrops fetalis associated with a nucleotide substitution in the erythrocyte beta-spectrin gene. J Clin Invest 1995; 95: 1174-1182.
    • (1995) J Clin Invest , vol.95 , pp. 1174-1182
    • Gallagher, P.G.1    Weed, S.A.2    Tse, W.T.3    Benoit, L.4    Morrow, J.S.5    Marchesi, S.L.6
  • 6
    • 4043053802 scopus 로고    scopus 로고
    • Hemophagocytic lymphohistiocytosis presenting with nonimmune hydrops fetalis
    • Malloy CA, Polinski C, Alkan S, Manera R, Challapalli M. Hemophagocytic lymphohistiocytosis presenting with nonimmune hydrops fetalis. J Perinatol 2004; 24: 458-460.
    • (2004) J Perinatol , vol.24 , pp. 458-460
    • Malloy, C.A.1    Polinski, C.2    Alkan, S.3    Manera, R.4    Challapalli, M.5
  • 8
    • 0026065540 scopus 로고
    • Diagnostic guidelines for hemophagocytic lymphohistiocytosis
    • The FHL Study Group of the Histiocyte Society
    • Henter JI, Elinder G, Ost A. Diagnostic guidelines for hemophagocytic lymphohistiocytosis. The FHL Study Group of the Histiocyte Society. Oncology 1991; 18: 29-33.
    • (1991) Oncology , vol.18 , pp. 29-33
    • Henter, J.I.1    Elinder, G.2    Ost, A.3
  • 9
    • 0031926347 scopus 로고    scopus 로고
    • Infection and malignancy-associated hemophagocytic syndromes: Secondary hemophagocytic lymphohistiocytosis
    • Janka G, Imashuku S, Elinder G, Schneider M, Henter J-I. Infection and malignancy-associated hemophagocytic syndromes: Secondary hemophagocytic lymphohistiocytosis. Hematol Oncol Clin North Am 1998; 12: 435-444.
    • (1998) Hematol Oncol Clin North Am , vol.12 , pp. 435-444
    • Janka, G.1    Imashuku, S.2    Elinder, G.3    Schneider, M.4    Henter, J.-I.5
  • 10
    • 0347064083 scopus 로고    scopus 로고
    • Modern management of children with hemophagocytic lymphohistiocytosis
    • Janka GE, Schneider EM. Modern management of children with hemophagocytic lymphohistiocytosis. Br J Haematol 2004; 124: 4-14.
    • (2004) Br J Haematol , vol.124 , pp. 4-14
    • Janka, G.E.1    Schneider, E.M.2
  • 11
    • 0032907043 scopus 로고    scopus 로고
    • Red blood cell membrane disorders
    • Tse WT, Lux SE. Red blood cell membrane disorders. Br J Haematol 1999; 104: 2-13.
    • (1999) Br J Haematol , vol.104 , pp. 2-13
    • Tse, W.T.1    Lux, S.E.2
  • 12
    • 2342609853 scopus 로고    scopus 로고
    • Update on the clinical spectrum and genetics of red blood cell membrane disorders
    • Gallagher PG. Update on the clinical spectrum and genetics of red blood cell membrane disorders. Curr Hematol Rep 2004; 3: 85-91.
    • (2004) Curr Hematol Rep , vol.3 , pp. 85-91
    • Gallagher, P.G.1
  • 13
    • 0029834849 scopus 로고    scopus 로고
    • Combination of two mutant α spectrin alleles underlies severe spherocytic hemolytic anemia
    • Wichterle H, Hanspal M, Palek J, Jarolim P. Combination of two mutant α spectrin alleles underlies severe spherocytic hemolytic anemia. J Clin Invest 1996; 98: 2300-2307.
    • (1996) J Clin Invest , vol.98 , pp. 2300-2307
    • Wichterle, H.1    Hanspal, M.2    Palek, J.3    Jarolim, P.4
  • 14
    • 0036660218 scopus 로고    scopus 로고
    • Hydrops fetalis-associated congenital dyserythropoietic anemia treated with intrauterine transfusions and bone marrow transplantation
    • Remacha AF, Badel I, Pujol-Moix N, Parra J, Muniz-Diaz E, Ginovart G et al. Hydrops fetalis-associated congenital dyserythropoietic anemia treated with intrauterine transfusions and bone marrow transplantation. Blood 2002; 100: 356-358.
    • (2002) Blood , vol.100 , pp. 356-358
    • Remacha, A.F.1    Badel, I.2    Pujol-Moix, N.3    Parra, J.4    Muniz-Diaz, E.5    Ginovart, G.6
  • 16
    • 13844255756 scopus 로고    scopus 로고
    • Review of hemophagocytic lymphohistiocytosis (HLH) in children with focus on Japanese experiences
    • Ishii E, Ohga S, Imashuku S, Kimura N, Ueda I, Morimoto A et al. Review of hemophagocytic lymphohistiocytosis (HLH) in children with focus on Japanese experiences. Crit Rev Oncol Hematol 2005; 53: 209-223.
    • (2005) Crit Rev Oncol Hematol , vol.53 , pp. 209-223
    • Ishii, E.1    Ohga, S.2    Imashuku, S.3    Kimura, N.4    Ueda, I.5    Morimoto, A.6
  • 17
    • 0025788568 scopus 로고
    • Sea blue histiocytes in the bone marrow of variant chronic granulomatous disease with residual monocyte NADPH-oxidase activity
    • Gahr M, Jendrossek V, Peters AM, Tegtmeyer F, Heyne K. Sea blue histiocytes in the bone marrow of variant chronic granulomatous disease with residual monocyte NADPH-oxidase activity. Br J Haematol 1991; 78: 278-280.
    • (1991) Br J Haematol , vol.78 , pp. 278-280
    • Gahr, M.1    Jendrossek, V.2    Peters, A.M.3    Tegtmeyer, F.4    Heyne, K.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.