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Epileptic encephalopathies and progressive neurodegeneration
被引:0
|作者:
Guerrini, R.
[1
,2
]
Conti, V.
[1
]
机构:
[1] IRCCS, Meyer Childrens Hosp, Neurosci Dept, Viale Pieraccini 24, I-50139 Florence, Italy
[2] Univ Florence, Dept Neurosci Psychol Drug Res & Child Hlth, Viale Pieraccini 6, I-50139 Florence, Italy
关键词:
SPTAN1;
V-ATPase;
DMXL2;
CDKL5;
TMEM63B;
MUTATIONS;
DISORDERS;
AUTOPHAGY;
D O I:
10.1016/j.neurol.2024.03.004
中图分类号:
R74 [神经病学与精神病学];
学科分类号:
摘要:
Developmental encephalopathies (DE), epileptic encephalopathies (EE) and developmental and epileptic encephalopathies (DEE) are overlapping neurodevelopmental disorders characterized by early -onset, often severe epileptic seizures, developmental delay, or regression and have multiple etiologies. Classical nosology in child neurology distinguished progressive and nonprogressive conditions. A progressive course with global cognitive worsening in DEE is usually attributed to severe seizures and electroencephalographic abnormalities whose deleterious effects interfere with developmental processes both in an apparently healthy brain and in an anatomically compromised one. Next generation sequencing and functional studies have helped identifying and characterizing clinical conditions, each with a broad spectrum of clinical and anatomic severity corresponding to a variable level of neurodegeneration, such that both a rapidly progressive course and considerably milder phenotypes with no obvious deterioration can be configured with mutations in the same gene. In this mini review, we present examples of genetic DEE that draw connections between neurodevelopmental and neurodegenerative disorders. (c) 2024 The Authors. Published by Elsevier Masson SAS. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
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页码:363 / 367
页数:5
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