已入深夜,您辛苦了!由于当前在线用户较少,发布求助请尽量完整地填写文献信息,科研通机器人24小时在线,伴您度过漫漫科研夜!祝你早点完成任务,早点休息,好梦!

An update on clinical, pathological, diagnostic, and therapeutic perspectives of childhood leukodystrophies

白质营养不良 人口 医学 白质脑病 白质 儿科 磁共振成像 病理 疾病 环境卫生 放射科
作者
Mahmoud Reza Ashrafi,Man Amanat,Masoud Garshasbi,Reyhaneh Kameli,Yalda Nilipour,Morteza Heidari,Zahra Rezaei,Ali Reza Tavasoli
出处
期刊:Expert Review of Neurotherapeutics [Taylor & Francis]
卷期号:20 (1): 65-84 被引量:62
标识
DOI:10.1080/14737175.2020.1699060
摘要

Introduction: Leukodystrophies constitute heterogenous group of rare heritable disorders primarily affecting the white matter of central nervous system. These conditions are often under-appreciated among physicians. The first clinical manifestations of leukodystrophies are often nonspecific and can occur in different ages from neonatal to late adulthood periods. The diagnosis is, therefore, challenging in most cases.Area covered: Herein, the authors discuss different aspects of leukodystrophies. The authors used MEDLINE, EMBASE, and GOOGLE SCHOLAR to provide an extensive update about epidemiology, classifications, pathology, clinical findings, diagnostic tools, and treatments of leukodystrophies. Comprehensive evaluation of clinical findings, brain magnetic resonance imaging, and genetic studies play the key roles in the early diagnosis of individuals with leukodystrophies. No cure is available for most heritable white matter disorders but symptomatic treatments can significantly decrease the burden of events. New genetic methods and stem cell transplantation are also under investigation to further increase the quality and duration of life in affected population.Expert opinion: The improvements in molecular diagnostic tools allow us to identify the meticulous underlying etiology of leukodystrophies and result in higher diagnostic rates, new classifications of leukodystrophies based on genetic information, and replacement of symptomatic managements with more specific targeted therapies.Abbreviations: 4H: Hypomyelination, hypogonadotropic hypogonadism and hypodontia; AAV: Adeno-associated virus; AD: autosomal dominant; AGS: Aicardi-Goutieres syndrome; ALSP: Axonal spheroids and pigmented glia; APGBD: Adult polyglucosan body disease; AR: autosomal recessive; ASO: Antisense oligonucleotide therapy; AxD: Alexander disease; BAEP: Brainstem auditory evoked potentials; CAA: Cerebral amyloid angiopathy; CADASIL: Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy; CARASAL: Cathepsin A–related arteriopathy with strokes and leukoencephalopathy; CARASIL: Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy; CGH: Comparative genomic hybridization; ClC2: Chloride Ion Channel 2; CMTX: Charcot-Marie-Tooth disease, X-linked; CMV: Cytomegalovirus; CNS: central nervous system; CRISP/Cas9: Clustered regularly interspaced short palindromic repeat/CRISPR-associated 9; gRNA: Guide RNA; CTX: Cerebrotendinous xanthomatosis; DNA: Deoxyribonucleic acid; DSB: Double strand breaks; DTI: Diffusion tensor imaging; FLAIR: Fluid attenuated inversion recovery; GAN: Giant axonal neuropathy; H-ABC: Hypomyelination with atrophy of basal ganglia and cerebellum; HBSL: Hypomyelination with brainstem and spinal cord involvement and leg spasticity; HCC: Hypomyelination with congenital cataracts; HEMS: Hypomyelination of early myelinated structures; HMG CoA: Hydroxy methylglutaryl CoA; HSCT: Hematopoietic stem cell transplant; iPSC: Induced pluripotent stem cells; KSS: Kearns-Sayre syndrome; L-2-HGA: L-2-hydroxy glutaric aciduria; LBSL: Leukoencephalopathy with brainstem and spinal cord involvement and elevated lactate; LCC: Leukoencephalopathy with calcifications and cysts; LTBL: Leukoencephalopathy with thalamus and brainstem involvement and high lactate; MELAS: Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke; MERRF: Myoclonic epilepsy with ragged red fibers; MLC: Megalencephalic leukoencephalopathy with subcortical cysts; MLD: metachromatic leukodystrophy; MRI: magnetic resonance imaging; NCL: Neuronal ceroid lipofuscinosis; NGS: Next generation sequencing; ODDD: Oculodentodigital dysplasia; PCWH: Peripheral demyelinating neuropathy-central-dysmyelinating leukodystrophy-Waardenburg syndrome-Hirschprung disease; PMD: Pelizaeus‐Merzbacher disease; PMDL: Pelizaeus-Merzbacher-like disease; RNA: Ribonucleic acid; TW: T-weighted; VWM: Vanishing white matter; WES: whole exome sequencing; WGS: whole genome sequencing; X-ALD: X-linked adrenoleukodystrophy; XLD: X-linked dominant; XLR: X-linked recessive
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
1秒前
molihuakai的应助被xjl采纳,获得10
3秒前
琪琪发布了新的文献求助10
3秒前
懒顾发布了新的文献求助10
4秒前
xiaohe发布了新的文献求助10
5秒前
wen发布了新的文献求助10
6秒前
6秒前
李爱国的应助被Aze采纳,获得10
8秒前
10秒前
酷波er的应助被Sci采纳,获得10
11秒前
Chiuchiu完成签到,获得积分10
13秒前
14秒前
科研通AI6.4的应助被LucyMartinez采纳,获得10
14秒前
Dliii完成签到 ,获得积分10
15秒前
aaa完成签到 ,获得积分10
17秒前
17秒前
leave完成签到,获得积分10
17秒前
18秒前
19秒前
完美世界的应助被wen采纳,获得10
20秒前
灰色头像完成签到,获得积分10
20秒前
20秒前
xjl发布了新的文献求助10
21秒前
热情思天完成签到,获得积分10
21秒前
WaRx发布了新的文献求助10
21秒前
111给111的求助进行了留言
22秒前
23秒前
xiaohe完成签到,获得积分20
24秒前
Ldj发布了新的文献求助10
24秒前
25秒前
英姑的应助被乐辰采纳,获得10
26秒前
情怀的应助被whisper采纳,获得30
26秒前
懒顾完成签到,获得积分20
27秒前
27秒前
28秒前
Akim的应助被泡芙采纳,获得10
29秒前
calm发布了新的文献求助10
32秒前
32秒前
英姑的应助被潜伏采纳,获得10
33秒前
Hello的应助被小叶不吃香菜采纳,获得10
33秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Aspects of Post-SPE Phonology 2000
CODESSA 2000
Rosenblum, Global Change Biology 800
Berberine regulates the TLR4 signaling pathway to suppress hypoxia-induced proliferation and migration of pulmonary arterial smooth muscle cells 520
Organizational Behavior 510
The Welfare Assembly Line: Public Servants in the Suffering City 500
热门求助领域 (近24小时)
化学 材料科学 医学 生物 计算机科学 工程类 纳米技术 有机化学 化学工程 内科学 物理 生物化学 复合材料 催化作用 细胞生物学 人工智能 心理学 无机化学 基因 遗传学
热门帖子
关注 科研通微信公众号,转发送积分 7852800
求助须知:如何正确求助?哪些是违规求助? 9371923
关于积分的说明 20680459
捐赠科研通 7450400
什么是DOI,文献DOI怎么找? 3344437
关于科研通互助平台的介绍 2487078
邀请新用户注册赠送积分活动 2367543