WordNet
- having or involving or consisting of more than one part or entity or individual; "multiple birth"; "multiple ownership"; "made multiple copies of the speech"; "his multiple achievements in public life"; "her multiple personalities"; "a pineapple is a multiple fruit"
- the product of a quantity by an integer; "36 is a multiple of 9"
- the 1st letter of the Roman alphabet (同)a
- the blood group whose red cells carry the A antigen (同)type_A, group A
- any group or radical of the form RCO- where R is an organic group; "an example of the acyl group is the acetyl group" (同)acyl_group
- a small molecule (not a protein but sometimes a vitamin) essential for the activity of some enzymes
PrepTutorEJDIC
- 〈U〉〈C〉(…の)(量・額などの)不足,欠乏《+『of』(『in』)+『名』》 / 〈C〉不足分,不足量,不足額 / 〈C〉(精神・肉体などの)欠陥
- 多数の部分(要素)から成る,複合の,複式の / 倍数
- answer / ampere
UpToDate Contents
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- 1. 脂質およびプリン代謝障害による代謝性ミオパチー metabolic myopathies caused by disorders of lipid and purine metabolism
- 2. グルコース-6-リン酸脱水素酵素欠損症の診断および治療 diagnosis and treatment of glucose 6 phosphate dehydrogenase deficiency
- 3. ヘキソースリン酸側路およびグルタチオン代謝疾患（グルコース-6-リン酸脱水素酵素欠損症を除く） disorders of the hexose monophosphate shunt and glutathione metabolism other than glucose 6 phosphate dehydrogenase deficiency
- 4. 水溶性ビタミンの概要 overview of water soluble vitamins
- 5. 乳酸脱水素酵素欠損症 lactate dehydrogenase deficiency
English Journal
- Fulminant lipid storage myopathy due to multiple acyl-coenzyme a dehydrogenase deficiency.
- Whitaker CH1, Felice KJ1, Silvers D2, Wu Q3.
- Muscle & nerve.Muscle Nerve.2015 Aug;52(2):289-93. doi: 10.1002/mus.24552. Epub 2015 Feb 11.
- INTRODUCTION: The lipid storage myopathies, primary carnitine deficiency, neutral lipid storage disease, and multiple acyl coenzyme A dehydrogenase deficiency (MADD), are progressive disorders that cause permanent weakness. These disorders of fatty acid metabolism and intracellular triglyceride degr
- PMID 25556768
- Spectrum analysis of common inherited metabolic diseases in Chinese patients screened and diagnosed by tandem mass spectrometry.
- Han L1, Han F, Ye J, Qiu W, Zhang H, Gao X, Wang Y, Ji W, Gu X.
- Journal of clinical laboratory analysis.J Clin Lab Anal.2015 Mar;29(2):162-8. doi: 10.1002/jcla.21745. Epub 2014 May 5.
- BACKGROUND: Information concerning inherited metabolic diseases in China is scarce. We investigated the prevalence and age distributions of amino acid, organic acid, and fatty acid oxidation disorders in Chinese patients.METHODS: Blood levels of amino acids and acylcarnitines (tandem mass spectromet
- PMID 24797655
- Glutaric aciduria type II presenting as myopathy and rhabdomyolysis in a teenager.
- Prasad M1, Hussain S2.
- Journal of child neurology.J Child Neurol.2015 Jan;30(1):96-9. doi: 10.1177/0883073813516676. Epub 2014 Jan 21.
- Late-onset glutaric aciduria type II has been described recently as a rare but treatable cause of proximal myopathy in teenagers and adults. It is an autosomal recessive disease affecting fatty acid, amino acid, and choline metabolism. This is usually a result of 2 defective flavoproteins: either el
- PMID 24453145
Japanese Journal
- Symmetric hypoplasia of the temporal cerebral lobes in an infant with glutaric aciduria type II (multiple acyl-coenzyme A dehydrogenase deficiency)
- STOCKLER S
- J Pediatr 124, 601-604, 1994
- NAID 30017462440
Related Links
- Multiple acyl coenzyme a dehydrogenase deficiency. On-line free medical diagnosis assistant. Ranked list of possible diseases from either several symptoms or a full patient history. A similarity measure between symptoms and ...
- "Multiple Acyl Coenzyme A Dehydrogenase Deficiency" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus, MeSH (Medical ... An autosomal recessive disorder of fatty acid oxidation, and branched ...
Related Pictures
★リンクテーブル★
| リンク元 | 「アミノ酸代謝異常症」「マルチプルアシルCoA脱水素酵素欠損症」「多種アシルCoA脱水素酵素欠損症」 |
| 関連記事 | 「deficiency」「A」「multiple」「Ad」「dehydrogenase」 |
「アミノ酸代謝異常症」
- 英
- aminoacidopathy, disorder of aminoacid metabolism disorders of amino acid metabolism
- 同
- アミノ酸代謝異常、先天性アミノ酸代謝異常症 先天性アミノ酸代謝異常 inborn error of amino acid metabolism
アミノ酸代謝異常症
- 国試で出たことが有るレベル
- 白化 albinism
- アルカプトン尿症 alkaptonuria
- 非ケトーシス型高グリシン血症 nonketotic hyperglycinemia
- 高ホモシステイン血症 hyperhomocysteinemia
- 高リジン血症 hyperlysinemia
- メープルシロップ尿症 maple syrup urine disease
- 多種アシルCoA脱水素酵素欠損症 multiple acyl-coenzyme A dehydrogenase deficiency
- マルチプルカルボキシラーゼ欠損症 multiple carboxylase deficiency
- フェニルケトン尿症 phenylketonuria
- プロピオン酸血症 propionic acidemia
- チロシン血症 tyrosinemia
- 先天性尿素回路代謝異常 inborn urea cycle disorder
アミノ酸代謝異常で痙攣を呈さないもの
「マルチプルアシルCoA脱水素酵素欠損症」
「多種アシルCoA脱水素酵素欠損症」
「deficiency」
- n.
- 不足、欠乏、欠失、欠如、欠損、不十分。栄養不足、栄養素欠乏、欠乏症。(遺伝子)(染色体内の)遺伝子欠失
- 欠けているもの、不足している物。不足分。不完全なもの、欠点のあるもの
- 関
- absence, agenesis, dearth, defect, defective, deficient, deficit, delete, deletion, deletional, depletion, deprivation, deprive, lack, miss, missing, morphological defect, paucity, scarce, scarcity, starve
「A」
「multiple」
- n.
- 倍数
- adj.