spinocerebellar disorder

脊髄小脳障害

WordNet

1. bring disorder to (同)disarray
2. a physical condition in which there is a disturbance of normal functioning; "the doctor prescribed some medicine for the disorder"; "everyone gets stomach upsets from time to time" (同)upset
3. a disturbance of the peace or of public order
4. not arranged in order (同)unordered

PrepTutorEJDIC

1. 〈U〉『無秩序』,混乱,乱雑(confusion) / 《しばしば複数形で》(社会的・政治的な)粉争,騒動 / 〈C〉(肉体的・精神的な)不調,異常,障害 / …‘の'秩序を乱す / 〈心身〉‘に'異常を起こさせる

UpToDate Contents

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• 1. 多系統萎縮症：臨床的特徴および診断 multiple system atrophy clinical features and diagnosis
• 2. 脊髄小脳変性症 the spinocerebellar ataxias
• 3. 全身疾患と関連した遺伝性ニューロパチー hereditary neuropathies associated with generalized disorders
• 4. レストレスレッグ症候群 restless legs syndrome
• 5. アルコールの慢性神経学的合併症の概要 overview of the chronic neurologic complications of alcohol

English Journal

• Different Mutations in ELOVL4 Affect Very Long Chain Fatty Acid Biosynthesis to Cause Variable Neurological Disorders in Humans.

• Agbaga MP1.
• Advances in experimental medicine and biology.Adv Exp Med Biol.2016;854:129-35. doi: 10.1007/978-3-319-17121-0_18.
• All mammalian cell membranes are characterized by amphipathic lipid molecules that interact with proteins to confer structural and functional properties on the cell. The predominant lipid species are phospholipids, glycolipids, sphingolipids and cholesterol. These lipids contain fatty acids with var
• PMID 26427403

• A patient with 41 CAG repeats in SCA17 presenting with parkinsonism and chorea.

• Park H1, Jeon BS2, Shin JH1, Park SH3.
• Parkinsonism & related disorders.Parkinsonism Relat Disord.2016 Jan;22:106-7. doi: 10.1016/j.parkreldis.2015.11.011. Epub 2015 Nov 14.
• PMID 26613966

• Mesenchymal stem cells attenuate peripheral neuronal degeneration in spinocerebellar ataxia type 1 knockin mice.

• Mieda T1, Suto N2, Iizuka A2, Matsuura S2, Iizuka H1, Takagishi K1, Nakamura K2, Hirai H2.
• Journal of neuroscience research.J Neurosci Res.2015 Dec 28. doi: 10.1002/jnr.23698. [Epub ahead of print]
• Spinocerebellar ataxia type 1 (SCA1) is a devastating neurodegenerative disorder in which an abnormally expanded polyglutamine tract is inserted into causative ataxin-1 proteins. We have previously shown that SCA1 knockin (SCA1-KI) mice over 6 months of age exhibit a degeneration of motor neuron axo
• PMID 26707550

Japanese Journal

• 5.脊髄小脳変性症

• Equilibrium Research 74(3), 159-165, 2015
• NAID 130005090983

• Psychology of patients with amyotrophic lateral sclerosis (ALS) compared with spinocerebellar degeneration, Parkinson's disease, and cerebrovascular disease

• The Kitasato medical journal 44(1), 12-16, 2014-03
• NAID 40020030145

• HSPの分子遺伝学と遺伝子診断

• 臨床神経学 54(12), 1016-1017, 2014
• NAID 130004921210

Related Links

• Ataxias and Cerebellar or Spinocerebellar Degeneration ...

What are Ataxias and Cerebellar or Spinocerebellar Degeneration? Ataxia often occurs when parts of the nervous system that control movement are damaged. People with ataxia experience a failure of muscle control in ...

• Spinocerebellar ataxia type 1 - Genetics Home Reference ...

This condition is inherited in an autosomal dominant pattern, which means one copy of the altered gene in each cell is sufficient to cause the disorder. An affected person usually inherits the altered gene from one affected ...

Related Pictures

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★リンクテーブル★

リンク元	「脊髄小脳障害」
関連記事	「disorder」

「脊髄小脳障害」

　　[★]

英

spinocerebellar disorder

「disorder」

　　[★]

• 障害：個人的苦痛や機能の障害があるので「疾病」とは言えるものの、その背景にある臓器障害がもう一つはっきりしない場合に用いられる。(PSY.9)

• n.

• an untidy state; a lack of order or organization (⇔order)
• violent behaviour of large groups of people
• an illness that cause a part of the body to stop functioning correctly

• 注意

disease <> illness <> disorder

• vt.

• 乱す、乱雑にする。(人)の(心身の)調子を狂わせる。

• vi.