序号(S/N) | 时间/Date | 类型/Type | 题目/Topic | 讲者/Speaker | 单位/Institution | ||
---|---|---|---|---|---|---|---|
1 | 07:30-08:00 | 专题报告 |
基底节病变的鉴别诊断 |
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2 | 08:00-08:30 | 专题报告 |
脑白质病变读片会 |
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序号(S/N) | 时间/Date | 类型/Type | 题目/Topic | 讲者/Speaker | 单位/Institution | ||
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1 | 08:30-08:55 | 青年英语病例演讲 |
Biotinidase deficiency:Case report and literature review |
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2 | 08:55-09:20 | 青年英语病例演讲 |
Spinal muscular atrophy with hypoplasia of the corpus callosum: a case report |
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3 | 09:20-09:45 | 青年英语病例演讲 |
Two pediatric patients with hemiplegic migraine presenting as acute encephalopathy: cases report and a literature review |
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4 | 09:45-10:10 | 青年英语病例演讲 |
A Case Report of Paediatric COVID-19-Related Acute Necrotizing Encephalopathy |
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5 | 10:10-10:20 |
休息 |
序号(S/N) | 时间/Date | 类型/Type | 题目/Topic | 讲者/Speaker | 单位/Institution | ||
---|---|---|---|---|---|---|---|
1 | 10:20-10:45 | 青年英语病例演讲 |
Diagnosis and treatment of a case of metabolic crisis caused by Carnitine palmitoyltransferase type IA deficiency |
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2 | 10:45-11:10 | 青年英语病例演讲 |
Anti-GAD65 antibody encephalitis in children: A case report and a review of the literature. |
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3 | 11:10-11:35 | 青年英语病例演讲 |
Clinical,radiological features and prognosis in pediatric patients with double positive anti-N-methyl-D-aspartate receptor antibody and anti-myelin oligodendrocyte glycoprotein antibody:A single center study |
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4 | 11:35-12:00 | 青年英语病例演讲 |
A Girl Who Had A Tough Journey |
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序号(S/N) | 时间/Date | 类型/Type | 题目/Topic | 讲者/Speaker | 单位/Institution | ||
---|---|---|---|---|---|---|---|
1 | 12:00-12:20 | 专题会 |
iWES在儿童神经内科遗传病应用的优势 |
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序号(S/N) | 时间/Date | 类型/Type | 题目/Topic | 讲者/Speaker | 单位/Institution | ||
---|---|---|---|---|---|---|---|
1 | 13:30-14:00 | 专题报告 |
代谢性神经-心脏共患疾病 |
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2 | 14:00-14:30 | 专题报告 |
溶酶体病的诊治进展 |
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3 | 14:30-14:40 | 大会发言 |
CACNA1C变异相关神经发育障碍的发病机制:线粒体功能障碍、线粒体自噬和凋亡是 |
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4 | 14:40-14:50 | 大会发言 |
中国Angelman综合征癫痫诊疗现状研究 |
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5 | 14:50-15:00 | 大会发言 |
单倍体异基因造血干细胞移植治疗儿童肾上腺脑白质营养不良的回顾性队列研究 |
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6 | 15:00-15:10 | 大会发言 |
髓鞘形成低下性脑白质营养TMEM63A基因突变患者临床遗传学特点分析 |
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7 | 15:10-15:20 | 大会发言 |
DNM1L基因变异所致线粒体过氧化物酶体裂殖缺陷型致死性脑病1型的临床特点总结及致病机制初步研究 |
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8 | 15:20-15:30 | 大会发言 |
PIGW基因变异致糖基磷脂酰肌醇缺乏症1例并文献复习 |
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9 | 15:30-15:40 |
休息 |
序号(S/N) | 时间/Date | 类型/Type | 题目/Topic | 讲者/Speaker | 单位/Institution | ||
---|---|---|---|---|---|---|---|
1 | 15:40-16:10 | 专题报告 |
急性脑病的罕见病因进展 |
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2 | 16:10-16:20 | 大会发言 |
对209例中国Leigh综合征患儿的生存分析 |
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3 | 16:20-16:30 | 大会发言 |
儿童原发性线粒体病的影像学特征和临床表型及基因型-影像表型相关性分析 |
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4 | 16:30-16:40 | 大会发言 |
44例AADCD患者临床分析及1例患者基因治疗随访 |
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5 | 16:40-16:50 | 大会发言 |
流式细胞术在诊断糖基磷脂酰肌醇缺陷相关疾病中的应用 |
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6 | 16:50-17:00 | 大会发言 |
MT-ND1的新发移码变异导致与MELAS综合征相关的线粒体复合物I缺陷 |
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7 | 17:00-17:10 | 大会发言 |
6例青春期起病的高同型半胱氨酸血症临床及基因研究 |
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