反復性ライ症候群
WordNet
- a pattern of symptoms indicative of some disease
- a complex of concurrent things; "every word has a syndrome of meanings"
PrepTutorEJDIC
- (疾患の徴候となる一群の)症徴候,症候群 / (事件・社会的状態などのパターンを示す)徴候形態
- 再発する;繰り返し起こる
- rheniumの化学記号
UpToDate Contents
全文を閲覧するには購読必要です。 To read the full text you will need to subscribe.
English Journal
- Dihydrolipoamide dehydrogenase deficiency: a still overlooked cause of recurrent acute liver failure and Reye-like syndrome.
- Brassier A1, Ottolenghi C, Boutron A, Bertrand AM, Valmary-Degano S, Cervoni JP, Chrétien D, Arnoux JB, Hubert L, Rabier D, Lacaille F, de Keyzer Y, Di Martino V, de Lonlay P.
- Molecular genetics and metabolism.Mol Genet Metab.2013 May;109(1):28-32. doi: 10.1016/j.ymgme.2013.01.017. Epub 2013 Feb 1.
- The causes of Reye-like syndrome are not completely understood. Dihydrolipoamide dehydrogenase (DLD or E3) deficiency is a rare metabolic disorder causing neurological or liver impairment. Specific changes in the levels of urinary and plasma metabolites are the hallmark of the classical form of the
- PMID 23478190
- Disorders of fatty acid oxidation.
- Tein I.
- Handbook of clinical neurology.Handb Clin Neurol.2013;113:1675-88. doi: 10.1016/B978-0-444-59565-2.00035-6.
- Recognition of fatty acid oxidation (FAO) disorders is important for the pediatric neurologist as they present with a spectrum of clinical disorders, including progressive lipid storage myopathy, recurrent myoglobinuria, neuropathy, progressive cardiomyopathy, recurrent hypoglycemic hypoketotic ence
- PMID 23622388
- Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome with stroke-like imaging presentation: clinical, biochemical and molecular analysis.
- Al-Hassnan ZN1, Rashed MS, Al-Dirbashi OY, Patay Z, Rahbeeni Z, Abu-Amero KK.
- Journal of the neurological sciences.J Neurol Sci.2008 Jan 15;264(1-2):187-94. Epub 2007 Sep 7.
- Hyperornithinemia-hyperammonemia-homocitrullinuria (HHH) syndrome is an autosomal recessive disorder caused by mutations in ORNT1 gene that encodes a mitochondrial ornithine transporter. It has variable clinical presentations with episodic hyperammonemia, liver dysfunction, and chronic neurological
- PMID 17825324
Japanese Journal
- 重症心身障害児・者の誤えんに対する声門閉鎖術の検討
- 工藤 典代,笹村 佳美,武宮 三三
- 日本気管食道科学会会報 49(3), 243-248, 1998
- … Eleven severely handicapped young patients with recurrent aspiration pneumonia were treated with the glottic closure procedure. … Their diseases were hypoxic encephalopathy, cerebral palsy, mitochondrial myopathies and after effects of Reye's syndrome. …
- NAID 130003448735
- 左片麻ひを合併し,特異なCT所見を呈したOrnithine transcarbamylase欠損症の1女児例
- 長谷川 潔,嘉山 益子,菊地 正宏,石沢 志信,成沢 邦明,多田 啓也,阿部 淳一郎,渡辺 修一
- 脳と発達 20(3), 232-236, 1988
- … 生検肝の微細脂肪浸潤よりReye症候群を疑ったが, 血清アミノ酸分析, 蛋白負荷試験よりomnithine transcarbamylase (OTC) 欠損症と診断した. …
- NAID 130004182398
- 筋カルニチン著減を伴ったPhosphoglvcomutase欠損症の1例
- 小林 順,市村 みゆき,杉江 陽子,杉江 秀夫,五十嵐 良雄
- 脳と発達 18(4), 310-315, 1986
- 原因不明の再発性嘔吐, 筋緊張低下, 傾眠傾向, 肝腫大, 体重増加不良, 著明な代謝性アシドーシスを呈した男児例を経験し, 血清および筋のカルニチンの著明な減少, 非ケトン性ジカルボン酸尿を認め, 全身型カルニチン欠損症を強く疑わせた. 筋組織化学所見では, 筋細胞内の脂肪の増加は軽度であったが, PAS染色にて筋鞘膜下の著明なグリコーゲン蓄積が見られた. 筋肉ホモジネートを用いたin vitr …
- NAID 130004182249
Related Links
- 1. Am J Dis Child. 1978 Nov;132(11):1097-9. Recurrent Reye's syndrome. Pichichero ME, McCabe ER. The clinical diagnosis of recurrent Reye's syndrome can be made only after a systemic exclusion of other diagnostic ...
- What is Reye's Syndrome? Reye's syndrome (RS) is primarily a children's disease, although it can occur at any age. It affects all organs of the body but is most harmful to the brain and the liver--causing an acute ...
★リンクテーブル★
[★]
- 英
- recurrent Reye syndrome, recurrent Reye's syndrome
- 同
- 再発性ライ症候群, 反復性Reye症候群
- 関
- ライ症候群
[★]
- 関
- iterative、recurrence、recurrently、regression、relapsing、repetitive
[★]
[★]