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See Latest ArticlesRapid full engraftment and successful immune reconstitution after allogeneic hematopoietic stem cell transplantation with reduced intensity conditioning in Omenn syndrome
Pediatric Transplantation, 08/20/09
Gozdzik J et al. – OS is a variant of SCID characterized by generalized erythroderma, alopecia, eosinophilia, and elevated IgE levels. It is fatal unless treated with allogeneic HSCT, which is the only curative approach. However, treatment related complications and graft rejection are major obstacles to the success of treatment. In this report, authors describe a patient with OS, complicated by prolonged cytomegalovirus infection, successfully treated by reduced intensity conditioning allogeneic HSCT from sibling donor.
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Neonatal seizures and Long QT Syndrome: A cardiocerebral channelopathy
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European Journal of Pediatrics, 11/05/09
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