Anemia and hepatosplenomegaly as presenting features in a child with rickets and secondary myelofibrosis

Journal of Pediatric Hematology/Oncology

Volumn 25, Issue 10, 2003, Pages 813-815

  Gruner, Barbara A ^a   DeNapoli, Thomas S ^c,e   Elshihabi, Said ^b   Britton, Howard A ^a   Langevin, Anne Marie ^a   Thomas, Paul J ^a   Weitman, Steven D ^a,d  

^a Department of Pediatrics ^*  (United States)

^b Long School of Medicine   (United States)

^c University of Texas Health Science Center   (United States)

^d CTRC Institute for Drug Development   (United States)

^e Santa Rosa Children's Hospital   (United States)

Author keywords

Anemia; Hepatomegaly; Myelofibrosis; Rickets; Splenomegaly; Vitamin D

Indexed keywords

ANEMIA; CASE REPORT; CLINICAL FEATURE; DIFFERENTIAL DIAGNOSIS; DISEASE ASSOCIATION; DISEASE SEVERITY; HEMOGLOBINOPATHY; HEMOLYTIC ANEMIA; HEPATOBLASTOMA; HEPATOSPLENOMEGALY; HISTIOCYTOSIS; HUMAN; INFANT; IRON DEFICIENCY ANEMIA; LEUKEMIA; LYMPHOMA; MALE; MYELOFIBROSIS; MYELOID METAPLASIA; NEUROBLASTOMA; PRIORITY JOURNAL; REVIEW; RICKETS;

ANEMIA; CALCITRIOL; DIAGNOSIS, DIFFERENTIAL; HEPATOMEGALY; HUMANS; INFANT; MALE; MYELOFIBROSIS; RICKETS; SPLENOMEGALY;

EID: 0141992772     PISSN: 10774114     EISSN: None     Source Type: Journal    
DOI: 10.1097/00043426-200310000-00015     Document Type: Review

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