Abstract:
BACKGROUND:Despite encouraging reports concerning the declining prevalence of iron deficiency, this easily preventable disorder is still an existing problem in presumably developed regions. OBJECTIVE:To evaluate the prevalence of iron deficiency and relevant anemia in children residing in Northern Greece and to study possible associations. DESIGN:3,100 children aged 8 months to 15 years were evaluated. Socioeconomic status was determined based on the parents' profession and place of residence. Nutrition habits were also evaluated. RESULTS:The incidence of iron deficiency was found to be 14% and that of iron deficiency anemia was 2.9%, with a higher prevalence in children younger than 2 years of age. The place of residence was the most significant factor in relation to the development of iron depletion in the children studied. Additional independent factors were revealed to be breast-feeding, meat-containing meal consumption and the consumption of non-home-cooked meals. CONCLUSION:Iron deficiency remains prevalent in Northern Greece, mainly affecting the vulnerable toddler group. Nutritional iron deficiency is still a severe public health problem even in what are considered to be developed regions. An improvement of dietary habits and an upgrading of semiurban areas should contribute substantially to decreasing the prevalence of iron depletion in Greek children.
journal_name
Acta Haematoljournal_title
Acta haematologicaauthors
Gompakis N,Economou M,Tsantali C,Kouloulias V,Keramida M,Athanasiou-Metaxa Mdoi
10.1159/000098273subject
Has Abstractpub_date
2007-01-01 00:00:00pages
200-4issue
4eissn
0001-5792issn
1421-9662pii
000098273journal_volume
117pub_type
杂志文章abstract::A patient with regional enteritis had received iron dextran for treatment of iron deficiency. Subsequently he developed a large (3.1 g/100 ml) IgG-K serum spike which had precipitin activity against dextran sulfate but not a variety of other antigens. There has been no evidence of multiple myeloma and the spike gradua...
journal_title:Acta haematologica
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journal_title:Acta haematologica
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journal_title:Acta haematologica
pub_type: 杂志文章
doi:10.1159/000208026
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journal_title:Acta haematologica
pub_type: 杂志文章
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pub_type: 杂志文章
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journal_title:Acta haematologica
pub_type: 杂志文章
doi:10.1159/000205198
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journal_title:Acta haematologica
pub_type: 杂志文章
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pub_type: 杂志文章,评审
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journal_title:Acta haematologica
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更新日期:2000-01-01 00:00:00
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journal_title:Acta haematologica
pub_type: 杂志文章,评审
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journal_title:Acta haematologica
pub_type: 杂志文章
doi:10.1159/000207709
更新日期:1978-01-01 00:00:00
abstract::In a 42-year-old Caucasian female, acute myelocytic leukemia (M2) presented as occlusion of the distal aorta and right iliac artery. She died after 10 days of respiratory failure. At postmortem examination the aortic wall contained multiple thrombi composed of fibrin and leukemic cells. There was no evidence of diffus...
journal_title:Acta haematologica
pub_type: 杂志文章
doi:10.1159/000206100
更新日期:1986-01-01 00:00:00
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journal_title:Acta haematologica
pub_type: 杂志文章
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更新日期:1986-01-01 00:00:00
abstract::A case of steroid-resistant acquired pure red-cell aplasia associated with a relative and absolute increase of TG cells is described. Removal of T cells enhanced erythroid colony and burst formation in vitro, and it is suggested that TG cells may be implicated in the pathogenesis of this case of acquired pure red-cell...
journal_title:Acta haematologica
pub_type: 杂志文章
doi:10.1159/000207191
更新日期:1981-01-01 00:00:00
abstract::Significant DNA polymorphisms have been reported in the beta-globin gene cluster of epsilon-G gamma-A gamma-psi beta-delta-beta-gene region, in normal (Hb AA) individuals and in patients with sickle cell anaemia (SCA). Investigations of the extent of the DNA polymorphisms in the beta A- and beta S-globin gene cluster ...
journal_title:Acta haematologica
pub_type: 杂志文章
doi:10.1159/000204653
更新日期:1992-01-01 00:00:00
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更新日期:2002-01-01 00:00:00
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pub_type: 杂志文章
doi:10.1159/000206155
更新日期:1985-01-01 00:00:00
abstract::Upper-extremity deep venous thrombosis (UEDVT) is an increasingly important clinical problem in children. These events are classified as primary or secondary, with the latter being the most common and usually associated with the presence of a central venous line. Among primary UEDVT, the so-called Paget-Schroetter syn...
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pub_type: 杂志文章
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更新日期:2006-01-01 00:00:00
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pub_type: 临床试验,杂志文章
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abstract::All-trans-retinoic acid (ATRA) combined with anthracyclines is currently the standard treatment for acute promyelocytic leukemia (APL). In elderly patients the presence of comorbidities, such as cardiomyopathy or different organ failures, often represents an absolute contraindication to standard chemotherapy. In this ...
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pub_type: 杂志文章
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更新日期:2007-01-01 00:00:00
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更新日期:1984-01-01 00:00:00
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abstract::Hypercalcemia is a significant feature of patients with active multiple myeloma (MM) with extensive bone disease. Among the causes of non-neoplastic hypercalcemia, primary hyperparathyroidism (PHPT) is one of the most common, leading to osteoporosis and bone fractures. Interestingly, some preclinical data indicate tha...
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pub_type:
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更新日期:2020-09-09 00:00:00