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Volumn 59, Issue 1, 2012, Pages 191-193

Hemophagocytic syndrome in a 4-month-old infant with biotinidase deficiency

Author keywords

Biotinidase deficiency; Children; Hemophagocytic lymphohistiocytosis

Indexed keywords

AMIKACIN; BIOTIN; BIOTINIDASE; IMMUNOGLOBULIN; MEROPENEM; TEICOPLANIN;

EID: 84861203610     PISSN: 15455009     EISSN: 15455017     Source Type: Journal    
DOI: 10.1002/pbc.23247     Document Type: Article
Times cited : (22)

References (20)
  • 1
    • 33845619137 scopus 로고    scopus 로고
    • HLH-2004: Diagnostic and therapeutic guidelines for hemophagocytic lymphohistiocytosis
    • Henter JI, Horne AC, Arico M, et al. HLH-2004: Diagnostic and therapeutic guidelines for hemophagocytic lymphohistiocytosis. Pediatr Blood Cancer 2007; 48: 124-131.
    • (2007) Pediatr Blood Cancer , vol.48 , pp. 124-131
    • Henter, J.I.1    Horne, A.C.2    Arico, M.3
  • 2
    • 33845878531 scopus 로고    scopus 로고
    • Hemophagocytic syndromes. Familial and acquired hemophagocytic lymphohistiocytosis
    • Janka GE. Hemophagocytic syndromes. Familial and acquired hemophagocytic lymphohistiocytosis. Eur J Pediatr 2007; 166: 95-109.
    • (2007) Eur J Pediatr , vol.166 , pp. 95-109
    • Janka, G.E.1
  • 3
    • 10744221563 scopus 로고    scopus 로고
    • Primary hemophagocytic lymphohistiocytosis in Turkish children
    • Gurgey A, Gogus S, Ozyurek E, et al. Primary hemophagocytic lymphohistiocytosis in Turkish children. Pediatr Hematol Oncol 2003; 20: 367-371.
    • (2003) Pediatr Hematol Oncol , vol.20 , pp. 367-371
    • Gurgey, A.1    Gogus, S.2    Ozyurek, E.3
  • 4
    • 78651404856 scopus 로고    scopus 로고
    • Clinical and laboratory data of primary hemophagocytic lymphohistiocytosis: A retrospective review of the Turkish Histiocyte Study Group
    • Fisgin T, Patiroglu T, Ozdemir A, et al. Clinical and laboratory data of primary hemophagocytic lymphohistiocytosis: A retrospective review of the Turkish Histiocyte Study Group. Turk J Hematol 2010; 4: 257-262.
    • (2010) Turk J Hematol , vol.4 , pp. 257-262
    • Fisgin, T.1    Patiroglu, T.2    Ozdemir, A.3
  • 5
    • 0033926347 scopus 로고    scopus 로고
    • Treatment of hemophagocytic lymphohistiocytosis with cyclosporine A and steroids in a boy with lysinuric protein intolerance
    • Bader-Meunier B, Perez N, Muller S. Treatment of hemophagocytic lymphohistiocytosis with cyclosporine A and steroids in a boy with lysinuric protein intolerance. J Pediatr 2000; 136: 134.
    • (2000) J Pediatr , vol.136 , pp. 134
    • Bader-Meunier, B.1    Perez, N.2    Muller, S.3
  • 6
    • 0038369135 scopus 로고    scopus 로고
    • Hemophagocytic syndrome following pseudomonas septicemia
    • Ermis B, Gardas F, Ceviz N, et al. Hemophagocytic syndrome following pseudomonas septicemia. Lancet Infect Dis 2003; 5: 287.
    • (2003) Lancet Infect Dis , vol.5 , pp. 287
    • Ermis, B.1    Gardas, F.2    Ceviz, N.3
  • 7
    • 34548684353 scopus 로고    scopus 로고
    • Hemophagocytic syndrome associated with high-dose lamotrigine
    • Gümüş H, Kumandaş S, Per H, et al. Hemophagocytic syndrome associated with high-dose lamotrigine. Pediatr Int 2007; 5: 672-673.
    • (2007) Pediatr Int , vol.5 , pp. 672-673
    • Gümüş, H.1    Kumandaş, S.2    Per, H.3
  • 8
    • 84861219660 scopus 로고    scopus 로고
    • Aplastic anemia presenting as hemophagocytic lymphohistiocytosis
    • Celkan T. Aplastic anemia presenting as hemophagocytic lymphohistiocytosis. Turk J Hematol 2010; 27: 38-42.
    • (2010) Turk J Hematol , vol.27 , pp. 38-42
    • Celkan, T.1
  • 9
    • 34547841478 scopus 로고    scopus 로고
    • Intense myelofibrosis in a child: Unusual result of EBV-associated hemophagocytic lymphohistiocytosis
    • Karapinar B, Yilmaz D, Aydinok Y, et al. Intense myelofibrosis in a child: Unusual result of EBV-associated hemophagocytic lymphohistiocytosis. Turk J Hematol 2007; 24: 32-35.
    • (2007) Turk J Hematol , vol.24 , pp. 32-35
    • Karapinar, B.1    Yilmaz, D.2    Aydinok, Y.3
  • 10
    • 10944273268 scopus 로고    scopus 로고
    • Pancytopenia, a rare hematologic manifestation of brucellosis in children
    • Karakukcu M, Patiroglu T, Ozdemir MA, et al. Pancytopenia, a rare hematologic manifestation of brucellosis in children. J Pediatr Hematol Oncol 2004; 26: 803-806.
    • (2004) J Pediatr Hematol Oncol , vol.26 , pp. 803-806
    • Karakukcu, M.1    Patiroglu, T.2    Ozdemir, M.A.3
  • 11
    • 0037746716 scopus 로고    scopus 로고
    • Successful treatment of infection-associated hemophagocytic syndrome with intravenous immunoglobulin
    • Oren H, Gulen H, Ucar C, et al. Successful treatment of infection-associated hemophagocytic syndrome with intravenous immunoglobulin. Turk J Hematol 2003; 20: 95-99.
    • (2003) Turk J Hematol , vol.20 , pp. 95-99
    • Oren, H.1    Gulen, H.2    Ucar, C.3
  • 12
    • 44949115389 scopus 로고    scopus 로고
    • Pearson syndrome associated with hemophagocytic syndrome in a child
    • Gumruk F, Kuskonmaz B, Coskun T. Pearson syndrome associated with hemophagocytic syndrome in a child. Turk J Hematol 2008; 25: 54-55.
    • (2008) Turk J Hematol , vol.25 , pp. 54-55
    • Gumruk, F.1    Kuskonmaz, B.2    Coskun, T.3
  • 13
    • 34548814973 scopus 로고    scopus 로고
    • Defective cytotoxic lymphocyte degranulation in syntaxin-11 deficient familial hemophagocytic lymphohistiocytosis 4 (FHL4) patients
    • Bryceson YT, Rudd E, Zheng C, et al. Defective cytotoxic lymphocyte degranulation in syntaxin-11 deficient familial hemophagocytic lymphohistiocytosis 4 (FHL4) patients. Blood 2007; 15: 1906-1915.
    • (2007) Blood , vol.15 , pp. 1906-1915
    • Bryceson, Y.T.1    Rudd, E.2    Zheng, C.3
  • 14
    • 0030869743 scopus 로고    scopus 로고
    • Multiple carboxylase deficiency: Inherited and acquired disorders of biotin metabolism
    • Baumgartner ER, Suormala T. Multiple carboxylase deficiency: Inherited and acquired disorders of biotin metabolism. Int J Vit Nutr Res 1997; 67: 377-384.
    • (1997) Int J Vit Nutr Res , vol.67 , pp. 377-384
    • Baumgartner, E.R.1    Suormala, T.2
  • 15
    • 0020525812 scopus 로고
    • Biotinidase deficiency: The enzymatic defect in late-onset multiple carboxylase deficiency
    • Wolf B, Grier RE, Allen RJ. Biotinidase deficiency: The enzymatic defect in late-onset multiple carboxylase deficiency. Clin Chim Acta 1983; 131: 273.
    • (1983) Clin Chim Acta , vol.131 , pp. 273
    • Wolf, B.1    Grier, R.E.2    Allen, R.J.3
  • 16
    • 53349154689 scopus 로고    scopus 로고
    • Biotin responsive disorders
    • Fernandes J, Saudubray JM, Walter JH, editors. Heidelberg: Springer Medizin Verlag;
    • Baumgartner ER, Suormala T. Biotin responsive disorders. In: Fernandes J, Saudubray JM, Walter JH, editors. Inborn metabolic diseases. Heidelberg: Springer Medizin Verlag; 2006. pp. 332-339.
    • (2006) Inborn metabolic diseases , pp. 332-339
    • Baumgartner, E.R.1    Suormala, T.2
  • 17
    • 0003114965 scopus 로고    scopus 로고
    • Disorders of biotin metabolism
    • Scriver RC, Beaudet AL, Sly WS, Valle D, editors. New York: McGraw-Hill;
    • Wolf B. Disorders of biotin metabolism. In: Scriver RC, Beaudet AL, Sly WS, Valle D, editors. The metabolic & molecular bases of inherited disease. New York: McGraw-Hill; 2001. pp. 3935-3962.
    • (2001) The metabolic & molecular bases of inherited disease , pp. 3935-3962
    • Wolf, B.1
  • 18
    • 0018748386 scopus 로고
    • Multiple biotin-dependent carboxylase deficiencies associated with defects in T-cell and B-cell immunity
    • Cowan MJ, Wara DW, Packman S, et al. Multiple biotin-dependent carboxylase deficiencies associated with defects in T-cell and B-cell immunity. Lancet 1979; 8134: 115-118.
    • (1979) Lancet , vol.8134 , pp. 115-118
    • Cowan, M.J.1    Wara, D.W.2    Packman, S.3
  • 19
    • 0024529635 scopus 로고
    • Biotin-responsive multiple carboxylase deficiency and immunodeficiency
    • Williams ML. Biotin-responsive multiple carboxylase deficiency and immunodeficiency. Curr Probl Dermatol 1989; 18: 89.
    • (1989) Curr Probl Dermatol , vol.18 , pp. 89
    • Williams, M.L.1
  • 20
    • 84861218571 scopus 로고    scopus 로고
    • Immunological problems
    • Hoffman GF, Zschocke J, Nyhan WL, editors. New York: Springer;
    • Mayatepek E. Immunological problems. In: Hoffman GF, Zschocke J, Nyhan WL, editors. Inherited metabolic diseases: A clinical approach. New York: Springer; 2010. pp. 243-248.
    • (2010) Inherited metabolic diseases: A clinical approach , pp. 243-248
    • Mayatepek, E.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.