家族性アポリポ蛋白B低βリポ蛋白血症、家族性アポリポタンパク質B低βリポタンパク質血症
WordNet
- relating to or having the characteristics of a family; "children of the same familial background"; "familial aggregation"
- occurring among members of a family usually by heredity; "an inherited disease"; "familial traits"; "genetically transmitted features" (同)genetic, hereditary, inherited, transmitted, transmissible
- the 2nd letter of the Roman alphabet (同)b
- the blood group whose red cells carry the B antigen (同)type_B, group B
- a hereditary disorder characterized by low levels of beta-lipoproteins and lipids and cholesterol
PrepTutorEJDIC
- 家族の,家族特有の / 違伝的な,血統にあらわれる
UpToDate Contents
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- 1. 遺伝性運動失調の概要 overview of the hereditary ataxias
- 2. LDLコレステロール代謝の遺伝性疾患 inherited disorders of ldl cholesterol metabolism
- 3. 脂質疾患に対するスクリーニング screening for lipid disorders
- 4. リポ蛋白の分類、代謝、およびアテローム性動脈硬化症における役割 lipoprotein classification metabolism and role in atherosclerosis
- 5. ネフローゼ症候群における脂質異常 lipid abnormalities in nephrotic syndrome
English Journal
- Rare and common variants of APOB and PCSK9 in Korean patients with extremely low low-density lipoprotein-cholesterol levels.
- Lee CJ1,2, Lee Y3, Park S1,2, Kang SM1,2, Jang Y1,2, Lee JH4, Lee SH1,2.
- PloS one.PLoS One.2017 Oct 16;12(10):e0186446. doi: 10.1371/journal.pone.0186446. eCollection 2017.
- PMID 29036232
- Threshold Effects of Circulating Angiopoietin-Like 3 Levels on Plasma Lipoproteins.
- Fazio S1, Minnier J2, Shapiro MD1, Tsimikas S3, Tarugi P4, Averna MR5, Arca M6, Tavori H1.
- The Journal of clinical endocrinology and metabolism.J Clin Endocrinol Metab.2017 Sep 1;102(9):3340-3348. doi: 10.1210/jc.2016-4043.
- PMID 28633452
- Clinical and biochemical characteristics of individuals with low cholesterol syndromes: A comparison between familial hypobetalipoproteinemia and familial combined hypolipidemia.
- Di Costanzo A1, Di Leo E2, Noto D3, Cefalù AB3, Minicocci I4, Polito L4, D'Erasmo L4, Cantisani V5, Spina R3, Tarugi P2, Averna M3, Arca M4.
- Journal of clinical lipidology.J Clin Lipidol.2017 Sep - Oct;11(5):1234-1242. doi: 10.1016/j.jacl.2017.06.013. Epub 2017 Jun 24.
- PMID 28733173
Japanese Journal
- Clinical Characterization of a Case with Familial Hypobetalipoproteinemia Caused by Apo B-76, a New Truncation of Apolipoprotein B, Combined with Apo E2/E2 Phenotype
- TAKAHASHI Kazuo,HIKITA Minoru,TAIRA Kouichi,KOBAYASHI Junji,BUJO Hideaki,SAITO Yasushi
- Internal medicine 40(10), 1015-1019, 2001-10
- … We report a 43-year-old Japanese man with hypobetalipoproteinemia likely due to apolipoprotein (apo) B-76, a new truncation of apo B, and with homozygousity for the apo E2 isoform. …
- NAID 10007002546
- Familial Hypobetalipoproteinemia Associated with Hypothyroidism
- MORIYAMA Kengo,TAKADA Yoichi,ARAKI Keiichi,MATSUNAGA Akira,SASAKI Jun,ARAKAWA Kikuo
- Internal medicine 34(9), 879-882, 1995-09
- … A 55-year-old Japanese woman with familial hypobetalipoproteinemia associated with hypothyroidism was admitted to the hospital because of orthopnea and congestive heart failure. … Thyroid function testing revealed hypothyroidism, but she exhibited low levels of serum cholesterol (111 mg/dl) and apolipoprotein (apo) B (48.5 mg/dl). …
- NAID 10006169794
Related Links
- Hypobetalipoproteinemia, Familial, Apolipoprotein B; Apolipoprotein B Deficiency. On-line free medical diagnosis assistant. Ranked list of possible diseases from either several symptoms or a full patient history. A similarity measure ... ...
- Familial hypobetalipoproteinemia (FHBL) is a disorder that impairs the body's ability to absorb and transport fats. This condition is characterized by low levels of a fat-like substance called cholesterol in the blood. The ...
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★リンクテーブル★
| リンク元 | 「家族性アポリポ蛋白B低βリポ蛋白血症」「家族性アポリポタンパク質B低βリポタンパク質血症」 |
| 関連記事 | 「B」「apolipoprotein」「familial」「apolipoproteins」 |
「家族性アポリポ蛋白B低βリポ蛋白血症」
「家族性アポリポタンパク質B低βリポタンパク質血症」
「B」
- 気管分岐部下緑
- 補体のalternative pathwayに関わる蛋白質
- Mg2+存在下でC3, B, Dが反応してC3bBbとなり、これがC3転換酵素(C3bBb)あるいはC5転換酵素(C3bBb3b)を形成する。これらはP(properdin)と結合して活性化し、それぞれC3、C5を活性化する
「apolipoprotein」
- 関
- apo
「familial」
- adj.
- 家族性の、家系性の、家族の