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[严重缺铁患者的畸形、异常和变异]

[Malformations, anomalies and variations in patients with severe iron deficiency].

作者信息

Reimann F, Erdogán G

出版信息

Blut. 1976 Jun;32(6):423-32. doi: 10.1007/BF01013882.

Abstract

In severe iron deficiency which frequently occurs in the population of Turkey, malformations, anomalies and variations are often observed. In 190 patients with severe iron deficiency of long duration such abnormalities could be found in 107 cases. The abnormal changes were of different character and occured in various parts of the body. In the majority multiple changes, ranging from 2 to 7 and more could be registered. 100 persons showing no iron deficiency and no anemia presented a much lower incidence of the same changes; in a second group of 54 patients suffering from a severe anemia without iron deficiency the incidence was still lower. These observations suggest that the occurrence of the abnormalities is closely connected with the iron deficiency. The character of the abnormal changes which are not susceptible to iron treatment are pointing to a prenatal origin. The diversity of the changes, the occurrence in various parts of the body and skeleton as well as the multiplicity of incidence are showing that they are due to impairment of the process of development in the embryonic organism. This view is supported by the results of the examination of the chromosomes. A distinct relation could be established between the incidence of the malformations and the occurrence of the chromosomal aberrations. As the iron deficiency in the Turkish population is mainly caused by an insufficient supply of iron with the food it is likely that by sufficient iron supply in pregnant women the incidence of malformations and anomalies caused by the iron deficiency can be prevented and by a general amelioration of the nutrition their occurrence in the population markedly reduced.

摘要

在土耳其人群中经常出现的严重缺铁情况下,常常观察到畸形、异常和变异。在190例长期严重缺铁的患者中,有107例发现了此类异常。这些异常变化具有不同的特征,发生在身体的各个部位。大多数情况下可记录到2至7种及更多的多种变化。100名无缺铁和贫血的人出现同样变化的发生率要低得多;在第二组54例患有严重贫血但无缺铁的患者中,发生率更低。这些观察结果表明,异常情况的发生与缺铁密切相关。对铁治疗无反应的异常变化特征表明其起源于产前。变化的多样性、在身体和骨骼各个部位的发生以及发生率的多重性表明,它们是由于胚胎有机体发育过程受损所致。这一观点得到了染色体检查结果的支持。畸形发生率与染色体畸变的发生之间可建立明显的关联。由于土耳其人群中的缺铁主要是由食物中铁供应不足引起的,因此孕妇充足的铁供应可能预防缺铁导致的畸形和异常的发生,并且通过总体营养改善,人群中此类情况的发生率可显著降低。

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