Treatment of congenital erythropoietic porphyria in children by allogeneic stem cell transplantion: A case report and review of the literature

Bone Marrow Transplantation

Volumn 27, Issue 1, 2001, Pages 101-105

  Shaw, P H ^a   Mancini, A J ^a   McConnell, J P ^b   Brown, D ^a   Kletzel, M ^a  

^a NORTHWESTERN UNIVERSITY   (United States)

^b MAYO CLINIC   (United States)

Author keywords

Bone marrow transplantation; Congenital erythropoietic porphyria; Porphyria; Stem cell transplantation

Indexed keywords

PORPHYRIN; UROPORPHYRIN; UROPORPHYRINOGEN III SYNTHASE;

ALLOGENIC BONE MARROW TRANSPLANTATION; ARTICLE; AUTOSOMAL RECESSIVE DISORDER; BONE DISEASE; CASE REPORT; CHILD; CLINICAL FEATURE; CONCENTRATION (PARAMETERS); CONGENITAL ERYTHROPOIETIC PORPHYRIA; ENZYME DEFICIENCY; ERYTHROCYTE; EXPERIENCE; FECES; HEMOLYTIC ANEMIA; HLA MATCHING; HUMAN; MALE; METABOLITE; PHOTOSENSITIVITY; PORPHYRIN METABOLISM; PRIORITY JOURNAL; PUBLICATION; REMISSION; SIBLING; SKIN DEFECT; SPLENOMEGALY; SURVIVAL; TOOTH DISEASE;

BLOOD DONORS; DISEASE-FREE SURVIVAL; HEMATOPOIETIC STEM CELL TRANSPLANTATION; HUMANS; INFANT; MALE; NUCLEAR FAMILY; PORPHYRIA, ERYTHROPOIETIC; TRANSPLANTATION, HOMOLOGOUS;

EID: 0035141108     PISSN: 02683369     EISSN: None     Source Type: Journal    
DOI: 10.1038/sj.bmt.1702738     Document Type: Article

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