Suppr超能文献

一名经分子学确诊的患有X连锁肾上腺脑白质营养不良症的坦桑尼亚男孩。

A Tanzanian Boy with Molecularly Confirmed X-Linked Adrenoleukodystrophy.

作者信息

Dekker M C J, Sadiq A M, Mc Larty R, Mbwasi R M, Willemsen M A A P, Waterham H R, Hamel B C

机构信息

Department of Paediatrics and Child Health, Kilimanjaro Christian Medical Centre, P.O. Box 3010, Moshi, Tanzania.

Department of Radiology, Kilimanjaro Christian Medical Centre, P.O. Box 3010, Moshi, Tanzania.

出版信息

Case Rep Genet. 2019 Dec 31;2019:6148425. doi: 10.1155/2019/6148425. eCollection 2019.

Abstract

Adrenoleukodystrophy (ALD) is an X-linked peroxisomal disorder with classical features, which can be also recognised in a low resource setting. It had been described in various populations across the globe, but very few cases have been reported from Africa. In a boy with features of a progressive central nervous system condition and adrenal failure, gene screening was performed based on a clinical history and basic radiological features which were compatible with ALD. A common mutation was identified in this patient, which is the first report of genetically confirmed ALD in Sub-Saharan Africa. ALD is likely under recognised in those areas where there is no neurologist. This genetic confirmation widens geographical distribution of -associated disease, and illustrates recognisability of this disorder, even when encountered in a low-resource environment.

摘要

肾上腺脑白质营养不良(ALD)是一种具有典型特征的X连锁过氧化物酶体疾病,在资源匮乏地区也可被识别。全球不同人群中均有相关描述,但非洲报道的病例很少。在一名具有进行性中枢神经系统疾病和肾上腺功能衰竭特征的男孩中,根据与ALD相符的临床病史和基本放射学特征进行了基因筛查。该患者中发现了一种常见突变,这是撒哈拉以南非洲地区首例经基因确诊的ALD报告。在没有神经科医生的地区,ALD可能未得到充分认识。这种基因确诊拓宽了相关疾病的地理分布范围,并表明即使在资源匮乏的环境中遇到这种疾病,也可识别。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e47/7011349/ac7ddd52ab47/CRIG2019-6148425.001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验