Myoclonus-dystonia/essential myoclonus

K. J. Peall; E. M.J. Foncke; M. A.J. Tijssen

doi:10.1016/B978-0-12-809324-5.00689-1

Myoclonus-dystonia/essential myoclonus

K. J. Peall
, E. M.J. Foncke
, M. A.J. Tijssen

Research output: Chapter in Book/Report/Conference proceeding › Chapter › Academic › peer-review

Abstract

Myoclonus Dystonia is a childhood-onset, hyperkinetic movement disorder characterized by upper body predominant myoclonus and dystonia. A proportion of cases are caused by autosomal dominantly inherited mutations to the epsilon-sarcoglycan gene (SGCE), located on the long-arm of chromosome 7 (7q21).

Original language	English
Title of host publication	The Curated Reference Collection in Neuroscience and Biobehavioral Psychology
Publisher	PERGAMON-ELSEVIER SCIENCE LTD
ISBN (Electronic)	9780128093245
DOIs	https://doi.org/10.1016/B978-0-12-809324-5.00689-1
Publication status	Published - 1-Jan-2016
Externally published	Yes

Keywords

Dystonia
DYT11
e-sarcoglycan
Essential myoclonus
Hereditary essential myoclonus
Inherited myoclonus-dystonia
Myoclonic dystonia
Myoclonus
Myoclonus-dystonia
Primary dystonia
Psychiatric symptoms

Access to Document

10.1016/B978-0-12-809324-5.00689-1

Handle.net

Persistent link

Cite this

@inbook{92b0a5eba93e40f297f45047347f9530,

title = "Myoclonus-dystonia/essential myoclonus",

abstract = "Myoclonus Dystonia is a childhood-onset, hyperkinetic movement disorder characterized by upper body predominant myoclonus and dystonia. A proportion of cases are caused by autosomal dominantly inherited mutations to the epsilon-sarcoglycan gene (SGCE), located on the long-arm of chromosome 7 (7q21).",

keywords = "Dystonia, DYT11, e-sarcoglycan, Essential myoclonus, Hereditary essential myoclonus, Inherited myoclonus-dystonia, Myoclonic dystonia, Myoclonus, Myoclonus-dystonia, Primary dystonia, Psychiatric symptoms",

author = "Peall, \{K. J.\} and Foncke, \{E. M.J.\} and Tijssen, \{M. A.J.\}",

year = "2016",

month = jan,

day = "1",

doi = "10.1016/B978-0-12-809324-5.00689-1",

language = "English",

booktitle = "The Curated Reference Collection in Neuroscience and Biobehavioral Psychology",

publisher = "PERGAMON-ELSEVIER SCIENCE LTD",

}

TY - CHAP

T1 - Myoclonus-dystonia/essential myoclonus

AU - Peall, K. J.

AU - Foncke, E. M.J.

AU - Tijssen, M. A.J.

PY - 2016/1/1

Y1 - 2016/1/1

N2 - Myoclonus Dystonia is a childhood-onset, hyperkinetic movement disorder characterized by upper body predominant myoclonus and dystonia. A proportion of cases are caused by autosomal dominantly inherited mutations to the epsilon-sarcoglycan gene (SGCE), located on the long-arm of chromosome 7 (7q21).

AB - Myoclonus Dystonia is a childhood-onset, hyperkinetic movement disorder characterized by upper body predominant myoclonus and dystonia. A proportion of cases are caused by autosomal dominantly inherited mutations to the epsilon-sarcoglycan gene (SGCE), located on the long-arm of chromosome 7 (7q21).

KW - Dystonia

KW - DYT11

KW - e-sarcoglycan

KW - Essential myoclonus

KW - Hereditary essential myoclonus

KW - Inherited myoclonus-dystonia

KW - Myoclonic dystonia

KW - Myoclonus

KW - Myoclonus-dystonia

KW - Primary dystonia

KW - Psychiatric symptoms

UR - https://www.scopus.com/pages/publications/85079568389

U2 - 10.1016/B978-0-12-809324-5.00689-1

DO - 10.1016/B978-0-12-809324-5.00689-1

M3 - Chapter

AN - SCOPUS:85079568389

BT - The Curated Reference Collection in Neuroscience and Biobehavioral Psychology

PB - PERGAMON-ELSEVIER SCIENCE LTD

ER -

Myoclonus-dystonia/essential myoclonus

Abstract

Keywords

Access to Document

Handle.net

Other files and links

Fingerprint

Myoclonus-Dystonia/Essential Myoclonus

Cite this