Childhood-onset hereditary spastic paraplegia and its treatable mimics.
Childhood-onset hereditary spastic paraplegia and its treatable mimics.
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DOI:
10.1016/j.ymgme.2021.06.006
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发表时间:
2022-12
影响因子:
3.8
通讯作者:
Pearl PL
中科院分区:
文献类型:
--
作者:
Ebrahimi-Fakhari D;Saffari A;Pearl PL
Early-onset forms of hereditary spastic paraplegia and inborn errors of metabolism that present with spastic diplegia are among the most common “mimics” of cerebral palsy. Early detection of these heterogenous genetic disorders can inform genetic counseling, anticipatory guidance, and improve outcomes, particularly where specific treatments exist. The diagnosis relies on clinical pattern recognition, biochemical testing, neuroimaging, and increasingly next-generation sequencing-based molecular testing. In this short review, we summarize the clinical and molecular understanding of: 1) childhood-onset and complex forms of hereditary spastic paraplegia (SPG5, SPG7, SPG11, SPG15, SPG35, SPG47, SPG48, SPG50, SPG51, SPG52) and, 2) the most common inborn errors of metabolism that present with phenotypes that resemble hereditary spastic paraplegia.
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DOI:
10.1056/nejmoa1700554
发表时间:
2017-10-26
期刊:
The New England journal of medicine
影响因子:
--
作者:
Eichler F;Duncan C;Musolino PL;Orchard PJ;De Oliveira S;Thrasher AJ;Armant M;Dansereau C;Lund TC;Miller WP;Raymond GV;Sankar R;Shah AJ;Sevin C;Gaspar HB;Gissen P;Amartino H;Bratkovic D;Smith NJC;Paker AM;Shamir E;O'Meara T;Davidson D;Aubourg P;Williams DA
通讯作者:
Williams DA
影响因子:
4.5
作者:
De Pace, Raffaella;Skirzewski, Miguel;Bonifacino, Juan S.
通讯作者:
Bonifacino, Juan S.
影响因子:
3.8
作者:
Carvalho, Daniel R.;Brum, Jaime M.;Pratesi, Riccardo
通讯作者:
Pratesi, Riccardo
影响因子:
--
作者:
Blackstone, Craig
通讯作者:
Blackstone, Craig
影响因子:
5.3
作者:
Chou, Cheng-Ta;Soong, Bing-Wen;Lee, Yi-Chung
通讯作者:
Lee, Yi-Chung