Clinical and biochemical footprints of inherited metabolic disease. XVI. Hematological abnormalities

被引:3
作者
Dunlea, Eoghan [1 ,2 ]
Crushell, Ellen [3 ,4 ]
Cotter, Melanie [1 ,4 ]
Blau, Nenad [5 ,7 ]
Ferreira, Carlos R. [6 ]
机构
[1] Childrens Hlth Ireland, Dept Haematol, Temple St, Dublin, Ireland
[2] Trinity Coll Dublin, Sch Med, Dublin, Ireland
[3] Childrens Hlth Ireland, Natl Ctr Inherited Metab Disorders, Temple St, Dublin, Ireland
[4] Univ Coll Dublin, Sch Med, Dublin, Ireland
[5] Univ Childrens Hosp, Div Metab, Zurich, Switzerland
[6] Natl Human Genome Res Inst, NIH, Bethesda, MD 20814 USA
[7] Univ Childrens Hosp, Div Metab, Steinwiesstr 75, CH-8032 Zurich, Switzerland
关键词
Bone marrow morphology; White blood cell morphology; Neutropenia; Thrombocytopenia; Pancytopenia; Anemia; Coagulation abnormalities; IEMbase; GLYCOGEN-STORAGE-DISEASE; VENOUS THROMBOEMBOLISM; DEFICIENCY; GUIDELINES; DIAGNOSIS; MANAGEMENT; MUTATION; GLYCOSYLATION; HEMOSTASIS; DISORDERS;
D O I
10.1016/j.ymgme.2023.107735
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Many classical inherited metabolic diseases (IMDs) are associated with significant hematological complications such as anemia or thrombosis. While these may not be the prominent presenting feature of these conditions, management of these issues is important for optimal outcomes in people with IMDs. Some disorders that are included in the nosology of inherited metabolic disorders, such as inherited disorders of red cell energy meta-bolism, have purely hematological features, and have typically been cared for by a hematologist. In the 16th issue of the Footprints series, we identified 265 IMDs associated with hematological abnormalities. We review the major hematological manifestations of IMDs, suggest further investigation of hematological findings, and discuss treatment options available for specific hematological complications of IMDs.
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页数:13
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