Clinicopathological Phenotype and Genetics of X-Linked Dystonia–Parkinsonism (XDP; DYT3; Lubag)

Clinicopathological Phenotype and Genetics of X-Linked Dystonia–Parkinsonism (XDP; DYT3; Lubag)

X-linked dystonia–parkinsonism (XDP; OMIM314250), also referred to as DYT3 dystonia or “Lubag” disease, was first described as an endemic disease in the Philippine island of Panay. XDP is an adult-onset movement disorder characterized by progressive and severe dystonia followed by overt parkinsonism...

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Bibliographic Details
Main Authors: Toshitaka Kawarai, Ryoma Morigaki, Ryuji Kaji, Satoshi Goto
Format: Article
Language:English
Published: MDPI AG 2017-06-01
Series:Brain Sciences
Subjects:
X-linked dystonia–parkinsonism
striatum
striosome
neurodegeneration
genetics
pathophysiology
Online Access:http://www.mdpi.com/2076-3425/7/7/72

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