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镰状细胞病和β地中海贫血患儿的牙科管理:综述

The dental management of children with sickle cell disease and beta-thalassaemia: a review.

作者信息

Duggal M S, Bedi R, Kinsey S E, Williams S A

机构信息

Division of Child Dental Health, Leeds Dental Institute, England.

出版信息

Int J Paediatr Dent. 1996 Dec;6(4):227-34. doi: 10.1111/j.1365-263x.1996.tb00250.x.

DOI:10.1111/j.1365-263x.1996.tb00250.x
PMID:9161189
Abstract

This paper reviews two groups of haemoglobinopathies: sickle cell disorders and beta-thalassaemias. The medical aspects and dental management of children with these conditions are discussed. These conditions are rare in the white indigenous population of the UK but affect a sizeable proportion of the minority ethnic community. Dentists need to be aware of the medical implications for patients who have these disorders and should co-ordinate their dental care accordingly.

摘要

本文综述了两组血红蛋白病

镰状细胞病和β地中海贫血。讨论了患有这些疾病的儿童的医学问题和牙科治疗。这些疾病在英国本土白人中很少见,但在少数族裔社区中影响了相当大的比例。牙医需要了解患有这些疾病的患者的医学影响,并应相应地协调他们的牙科护理。

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Correlation between maxillofacial radiographic features and systemic severity as sickle cell disease severity predictor.颌面影像学特征与系统性严重程度的相关性作为镰状细胞病严重程度的预测指标。
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Orthodontic management of traumatic avulsion of permanent incisors in a child with sickle cell anaemia: a case report.镰状细胞贫血患儿恒牙外伤性完全脱出的正畸治疗:一例报告
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