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1998年奥克兰地区患有严重维生素D缺乏性佝偻病儿童的特征。

Characteristics of children with florid vitamin D deficient rickets in the Auckland region in 1998.

作者信息

Blok B H, Grant C C, McNeil A R, Reid I R

机构信息

Department of Chemical Pathology, Auckland Hospital.

出版信息

N Z Med J. 2000 Sep 8;113(1117):374-6.

PMID:11050902
Abstract

AIM

To describe the characteristics of children with vitamin D deficiency rickets and identify common features and predisposing factors.

METHODS

A review of the clinical notes of all children less than five years of age with radiological evidence of rickets and serum 25-hydroxyvitamin D levels of less than 10 micrograms/L. Patients were identified by searching all low vitamin D levels performed at the Endocrinology laboratory at Auckland Hospital and children presenting to the Starship Childrens' Hospital with rickets in 1998.

RESULTS

In 1998, there were eighteen children (ten males and eight females) with vitamin D deficient rickets. The age range was 3 to 36 months with a median of 12 months. There were twelve children of Indian ethnic origin, one Maori, one Tongan, one Western Samoan, one Ethiopian, one Moroccan and one Indonesian. All children had an elevated alkaline phosphatase level and most had very low serum 25-hydroxyvitamin D levels (< or = 5 micrograms/L), and over half were hypocalcaemic. The common presenting features were delayed walking and bowed legs, swollen wrists or ankles, hypocalcaemic seizure, incidental radiological abnormalities and failure to thrive.

CONCLUSIONS

There are a significant number of children in Auckland presenting with florid clinical rickets. The majority with vitamin D deficient rickets in this survey were of Indian ethnic origin. Strategies are needed to detect children at risk of vitamin D deficiency and supplement them with vitamin D.

摘要

目的

描述维生素D缺乏性佝偻病患儿的特征,确定其共同特点和易感因素。

方法

回顾所有年龄小于5岁、有佝偻病放射学证据且血清25-羟维生素D水平低于10微克/升的患儿的临床记录。通过检索奥克兰医院内分泌实验室所有低维生素D水平检测结果以及1998年在星舰儿童医院就诊的佝偻病患儿来确定研究对象。

结果

1998年,有18例维生素D缺乏性佝偻病患儿(10例男性,8例女性)。年龄范围为3至36个月,中位数为12个月。其中有12名印度裔儿童,1名毛利人,1名汤加人,1名西萨摩亚人,1名埃塞俄比亚人,1名摩洛哥人和1名印度尼西亚人。所有患儿碱性磷酸酶水平均升高,大多数患儿血清25-羟维生素D水平极低(≤5微克/升),超过半数患儿存在低钙血症。常见的临床表现为学步延迟、下肢弯曲、手腕或脚踝肿胀、低钙惊厥、偶然发现的放射学异常以及生长发育迟缓。

结论

奥克兰有相当数量的儿童患有明显的临床佝偻病。本次调查中大多数维生素D缺乏性佝偻病患儿为印度裔。需要采取策略来检测有维生素D缺乏风险的儿童并为其补充维生素D。

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