Outcomes Following Hematopoietic Cell Transplantation for Wiskott Aldrich Syndrome

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منابع مشابه

[Hematopoietic stem cell transplantation for patients with Wiskott-Aldrich syndrome].

BACKGROUND Wiskott-Aldrich syndrome (WAS) is an X linked congenital disease that presents as eczema, thrombocytopenia and immune deficiency. The only curative procedure for this illness is hematopoietic stem cell transplant (HSCT), preferably from a healthy HLA identical sibling donor. Cord blood is becoming an excellent alternative as stem cell source from unrelated donors. AIM To report our...

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Brief report Correction of the murine Wiskott-Aldrich syndrome phenotype by hematopoietic stem cell transplantation

Allogeneic hematopoietic stem cell transplantation (HSCT) corrects the WiskottAldrich syndrome (WAS) phenotype. However, the toxicity and mortality frequently associated with this approach warrant the exploration of new therapeutic strategies. Transplantation studies of a murine model of WAS deficiency have been limited by the occurrence of a radiationinduced fatal exacerbation of a preexisting...

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Correction of the murine Wiskott-Aldrich syndrome phenotype by hematopoietic stem cell transplantation.

Allogeneic hematopoietic stem cell transplantation (HSCT) corrects the Wiskott-Aldrich syndrome (WAS) phenotype. However, the toxicity and mortality frequently associated with this approach warrant the exploration of new therapeutic strategies. Transplantation studies of a murine model of WAS deficiency have been limited by the occurrence of a radiation-induced fatal exacerbation of a pre-exist...

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Hematopoietic Cells in Carriers of Wiskott-Aldrich Syndrome

The Wiskott-Aldrich syndrome (WAS) is an X-linked (Xpll.22) recessive immunodeficiency syndrome characterized by susceptibility to opportunistic and pyogenic infections, thrombocytopenia, and eczema. Previous studies of obligate carriers of WAS documented that nonrandom inactivation of the X chromosome carrying the defective gene is observed in all peripheral blood cells. The existence of b...

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[The Wiskott-Aldrich syndrome].

can occur, the observed improvement cannot necessarily b)e attributed to the transfer factor. However, in two patients repeated remissions consistently followed transfer factor administration on repeated occasions. This included freedom from infections, regression of splenomegaly, and clearing of eczema. An unexpected finding was a decrease in bleeding in 3 of the 10 patients who had bleeding. ...

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ژورنال

عنوان ژورنال: Biology of Blood and Marrow Transplantation

سال: 2011

ISSN: 1083-8791

DOI: 10.1016/j.bbmt.2010.12.466