Familial severe congenital neutropenia associated with infantile osteoporosis: A new entity

Autor:	Jacob M. Rowe, L.C. Hofbauer, Amos Etzioni, M. Ben-Arush, S. Ish-Shalom, O. Koc, Ronit Elhasid
Rok vydání:	2002
Předmět:	Male Neutropenia Filgrastim Bone disease Pancytopenia Osteoporosis Receptors Cytoplasmic and Nuclear Genes Recessive Bioinformatics Receptors Tumor Necrosis Factor Bone remodeling Consanguinity Osteoprotegerin Agammaglobulinemia Recurrence Granulocyte Colony-Stimulating Factor medicine Humans Congenital Neutropenia Cells Cultured Glycoproteins Peripheral Blood Stem Cell Transplantation Membrane Glycoproteins Leukopenia Receptor Activator of Nuclear Factor-kappa B business.industry RANK Ligand fungi Immunoglobulins Intravenous Hematology Bone fracture Fibroblasts medicine.disease Recombinant Proteins Failure to Thrive Pedigree Fractures Spontaneous Child Preschool Immunology Bone Remodeling medicine.symptom Carrier Proteins business
Zdroj:	American Journal of Hematology. 72:34-37
ISSN:	1096-8652 0361-8609
DOI:	10.1002/ajh.10261
Popis:	A new entity manifested by severe congenital neutropenia associated with osteoporosis and recurrent bone fracture is described in a family. A possible role for a new recognized cytokine system involved in bone remodeling, the osteoprotegerin/receptor activator of nuclear factor-κB ligand, is suggested. Am. J. Hematol. 72:34–37, 2003. © 2002 Wiley-Liss, Inc.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3f83ee991c5e85ee78bfbf621308e970 https://doi.org/10.1002/ajh.10261 Zobrazit plný text záznamu Plný text