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出典(authority):フリー百科事典『ウィキペディア（Wikipedia）』「2016/05/26 12:20:15」(JST)

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Choreoathetosis is the occurrence of involuntary movements in a combination of chorea (irregular migrating contractions) and athetosis (twisting and writhing).

It is caused by many different diseases and agents. It is a symptom of several diseases, including Lesch-Nyhan Syndrome, phenylketonuria, and Huntington disease.

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etiology

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1. ジストニアの分類および評価 classification and evaluation of dystonia
2. 小児における運動過多な運動障害 hyperkinetic movement disorders in children
3. 遅発性ジスキネジア：臨床的特徴および診断 tardive dyskinesia clinical features and diagnosis
4. 大脳皮質基底核変性症 corticobasal degeneration
5. 脳性麻痺の診断 diagnosis of cerebral palsy

English Journal

A Mutation in a Ganglioside Biosynthetic Enzyme, ST3GAL5, Results in Salt & Pepper Syndrome, a Neurocutaneous Disorder with Altered Glycolipid and Glycoprotein Glycosylation.

Boccuto L, Aoki K, Flanagan-Steet H, Chen CF, Fan X, Bartel F, Petukh M, Pittman A, Saul R, Chaubey A, Alexov E, Tiemeyer M, Steet R, Schwartz CE.SourceGreenwood Genetic Center, Greenwood, SC, 29646, USA.
Human molecular genetics.Hum Mol Genet.2013 Sep 10. [Epub ahead of print]
"Salt & Pepper" syndrome is an autosomal recessive condition characterized by severe intellectual disability, epilepsy, scoliosis, choreoathetosis, dysmorphic facial features, and altered dermal pigmentation. High density SNP array analysis performed on siblings first described with this syndrom
PMID 24026681

N-methyl-D-aspartate receptor antibodies in post-herpes simplex virus encephalitis neurological relapse.

Hacohen Y, Deiva K, Pettingill P, Waters P, Siddiqui A, Chretien P, Menson E, Lin JP, Tardieu M, Vincent A, Lim MJ.SourceNuffield Department of Clinical Neurosciences, John Radcliffe Hospital, University of Oxford, Oxford, United Kingdom.
Movement disorders : official journal of the Movement Disorder Society.Mov Disord.2013 Sep 6. doi: 10.1002/mds.25626. [Epub ahead of print]
Herpes simplex virus encephalitis (HSVE) is a devastating condition that relapses, often with a chorea in children, despite adequate antiviral treatment. At relapse, evidence of viral replication is frequently absent, suggesting that the relapse may be immune-mediated. Seven children who had a neuro
PMID 24014096

Renal transplantation in 4 patients with methylmalonic aciduria: A cell therapy for metabolic disease.

Brassier A, Boyer O, Valayannopoulos V, Ottolenghi C, Krug P, Cosson MA, Touati G, Arnoux JB, Barbier V, Bahi-Buisson N, Desguerre I, Charbit M, Benoist JF, Dupic L, Aigrain Y, Blanc T, Salomon R, Rabier D, Guest G, de Lonlay P, Niaudet P.SourceCentre de Référence des Maladies Héréditaires du Métabolisme de l'Enfant et de l'Adulte (MaMEA), Hôpital Necker-Enfants Malades, Université Paris Descartes, Institut Imagine, France.
Molecular genetics and metabolism.Mol Genet Metab.2013 Sep-Oct;110(1-2):106-10. doi: 10.1016/j.ymgme.2013.05.001. Epub 2013 May 14.
INTRODUCTION: Patients with methylmalonic acidemia (MMA) may develop many complications despite medical treatment, in particular, severe central nervous system damage and chronic kidney disease (CKD). A kidney transplant may partially correct the metabolic dysfunctions. Liver, kidney and combined li
PMID 23751327

Japanese Journal

Effectiveness of Oral Iron Chelator Treatment with Deferasirox in an Aceruloplasminemia Patient with a Novel Ceruloplasmin Gene Mutation

Suzuki Yasuhiro,Yoshida Kosuke,Aburakawa Yoko,Kuroda Kenji,Kimura Takashi,Terada Tatsuhiro,Kono Satoshi,Miyajima Hiroaki,Yahara Osamu
Internal Medicine 52(13), 1527-1530, 2013
… A 59-year-old man presented with refractory anemia, choreoathetosis in the left upper extremity, an unsteady gait and cognitive dysfunction. … The oral chelator deferasirox was effective in treating the left-side choreoathetosis and unsteady gait. …
NAID 130003365686

A Japanese Adult Case of Megalencephalic Leukoencephalopathy with Subcortical Cysts with a Good Long-term Prognosis

Koyama Shingo,Kawanami Toru,Arawaka Shigeki,Wada Manabu,Kato Takeo
Internal Medicine 51(5), 503-506, 2012
Megalencephalic leukoencephalopathy with subcortical cysts (MLC) is a recently recognized neurological disease, and mutations in the MLC1 gene have been identified as the cause of the disorder. A 54-y …
NAID 130002061903