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. 1995 Mar;72(3):241–242. doi: 10.1136/adc.72.3.241

Paroxysmal nocturnal haemoglobinuria and Budd-Chiari syndrome.

H A Wyatt 1, A P Mowat 1, M Layton 1
PMCID: PMC1511044  PMID: 7741575

Abstract

An 11 year old boy developed pancytopenia, haemolysis, and Budd-Chiari syndrome. The venous thrombosis extended to involve other intra-abdominal vessels before paroxysmal nocturnal haemoglobinuria was recognised as the underlying haematological abnormality. Earlier diagnosis would have made curative bone marrow transplantation a possibility.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Kawahara K., Witherspoon R. P., Storb R. Marrow transplantation for paroxysmal nocturnal hemoglobinuria. Am J Hematol. 1992 Apr;39(4):283–288. doi: 10.1002/ajh.2830390409. [DOI] [PubMed] [Google Scholar]
  2. Rosse W. F. Phosphatidylinositol-linked proteins and paroxysmal nocturnal hemoglobinuria. Blood. 1990 Apr 15;75(8):1595–1601. [PubMed] [Google Scholar]
  3. Takeda J., Miyata T., Kawagoe K., Iida Y., Endo Y., Fujita T., Takahashi M., Kitani T., Kinoshita T. Deficiency of the GPI anchor caused by a somatic mutation of the PIG-A gene in paroxysmal nocturnal hemoglobinuria. Cell. 1993 May 21;73(4):703–711. doi: 10.1016/0092-8674(93)90250-t. [DOI] [PubMed] [Google Scholar]

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