Familial infantile myelofibrosis as an autosomal recessive disorder: Preponderance among children from Saudi Arabia [2]

Pediatric Hematology and Oncology

Volumn 23, Issue 5, 2006, Pages 453-454

  Rossbach, Hans Christoph ^a,b  

^a UNIVERSITY OF SOUTH FLORIDA   (United States)

^b St Joseph's Children's Hospital of Tampa   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

AUTOSOMAL RECESSIVE DISORDER; CHILD; EXTRAMEDULLARY HEMATOPOIESIS; HUMAN; INHERITANCE; LETTER; MYELOFIBROSIS; MYELOID METAPLASIA; MYELOPHTHISIC ANEMIA; PUBLICATION; SAUDI ARABIA;

CHILD; GENES, RECESSIVE; HUMANS; MYELOFIBROSIS; MYELOID METAPLASIA; PREVALENCE; SAUDI ARABIA;

EID: 33746833594     PISSN: 08880018     EISSN: 15210669     Source Type: Journal    
DOI: 10.1080/08880010600623240     Document Type: Letter

References (4)

1. Sieff CA, Malleson P. Familial myelofibrosis. Arch Dis Childhood. 1980;55:888-893.
2. Sheikha A. Fatal familial infantile myelofibrosis. J Pediatr Hematol Oncol. 2004;26:164-168.
3. Mallouh AA, Sa'di AR. Agnogenic myeloid metaplasia in children. AJDC. 1992;146:965-967.
4. Rossbach HC, Grana NH, Chamizo W, et al. Successful allogeneic bone marrow transplantation for agnogenic myeloid metaplasia in a three-year-old boy. J Pediatr Hematol Oncol. 1996;18:213-215.