家族性高リポ蛋白血症IV型
WordNet
- write by means of a keyboard with types; "type the acceptance letter, please" (同)typewrite
- a small metal block bearing a raised character on one end; produces a printed character when inked and pressed on paper; "he dropped a case of type, so they made him pick them up"
- (biology) the taxonomic group whose characteristics are used to define the next higher taxon
- a subdivision of a particular kind of thing; "what type of sculpture do you prefer?"
- all of the tokens of the same symbol; "the word `element contains five different types of character"
- printed characters; "small type is hard to read"
- identify as belonging to a certain type; "Such people can practically be typed" (同)typecast
- 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 9th letter of the Roman alphabet (同)i
- any of various disorders of lipoprotein and cholesterol metabolism that result in high levels of lipoprotein and cholesterol in the circulating blood
- writing done with a typewriter (同)typewriting
PrepTutorEJDIC
- 〈C〉(…の)『型』,タイプ,類型,種類(kind)《+of+名》 / 〈C〉(その種類の特質を最もよく表している)『典型』,手本,模範《+of+名》 / 〈U〉《集合的に》活字;〈C〉(1個の)活字 / 〈U〉(印刷された)字体,活字 / 〈C〉(貨幣・メダルなどの)模様,図柄 / 〈C〉血液型(blood group) / …‘を'タイプに打つ / (…として)…‘を'分類する《+名+as+名(doing)》 / …‘の'型を決める / タイプライターを打つ
- 家族の,家族特有の / 違伝的な,血統にあらわれる
- 『私は』私が
- iodineの化学記号
Wikipedia preview
出典(authority):フリー百科事典『ウィキペディア(Wikipedia)』「2017/09/06 07:08:19」(JST)
[Wiki en表示]
Familial hypertriglyceridemia is an autosomal dominant condition occurring in approximately 1% of the population.[1] Triglyceride levels, but not cholesterol, are elevated as a result of excess hepatic production of VLDL or heterozygous LPL deficiency. The condition is associated with premature coronary disease, though treatment sometimes differs from hypercholesterolemia. Affected individuals are at risk for chylomicronemia syndrome, characterized by elevated chylomicrons in the blood. They are also at risk of pancreatitis, especially when triglyceride levels exceed 1000mg/dL.
See also
- Primary hyperlipoproteinemia
- Familial apoprotein CII deficiency
- Skin lesion
References
- ^ Boman H,Hazzard WR, AlbersJJ, et ah Frequency of monogenic forms of hyperlipidemia in a normal population. AmJ ttum Genet 27:19A,1975. [1]
Inborn error of lipid metabolism: dyslipidemia (E78, 272.0–272.6)
|
Hyperlipidemia |
- Hypercholesterolemia/Hypertriglyceridemia
- Lipoprotein lipase deficiency/Type Ia
- Familial apoprotein CII deficiency/Type Ib
- Familial hypercholesterolemia/Type IIa
- Combined hyperlipidemia/Type IIb
- Familial dysbetalipoproteinemia/Type III
- Familial hypertriglyceridemia/Type IV
- Xanthoma/Xanthomatosis
|
Hypolipoproteinemia |
Hypoalphalipoproteinemia/HDL |
- Lecithin cholesterol acyltransferase deficiency
- Tangier disease
|
Hypobetalipoproteinemia/LDL |
- Abetalipoproteinemia
- Apolipoprotein B deficiency
- Chylomicron retention disease
|
|
Lipodystrophy |
- Barraquer–Simons syndrome
|
Other |
- Lipomatosis
- Adiposis dolorosa
- Lipoid proteinosis
- APOA1 familial renal amyloidosis
|
UpToDate Contents
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English Journal
- Clinical and molecular characterization of a novel PLIN1 frameshift mutation identified in patients with familial partial lipodystrophy.
- Kozusko K1, Tsang VH2, Bottomley W3, Cho YH4, Gandotra S5, Mimmack M1, Lim K1, Isaac I1, Patel S1, Saudek V1, O'Rahilly S1, Srinivasan S6, Greenfield JR7, Barroso I3, Campbell LV8, Savage DB9.
- Diabetes.Diabetes.2015 Jan;64(1):299-310. doi: 10.2337/db14-0104. Epub 2014 Aug 11.
- Perilipin 1 is a lipid droplet coat protein predominantly expressed in adipocytes, where it inhibits basal and facilitates stimulated lipolysis. Loss-of-function mutations in the PLIN1 gene were recently reported in patients with a novel subtype of familial partial lipodystrophy, designated as FPLD4
- PMID 25114292
- [Two forms of familial hypercholesterolemia: differences in cardiovascular risk factors, cardiac and extracardiac atherosclerosis].
- Vogt A1, Keller C1, Heigl C2, Weiss N3, Zöllner N1.
- Deutsche medizinische Wochenschrift (1946).Dtsch Med Wochenschr.2014 Dec;139(50):2573-7. doi: 10.1055/s-0034-1387237. Epub 2014 Aug 15.
- BACKGROUND AND AIM: The monogenetic hypercholesterolemias (HC) are associated with a very high risk of premature coronary heart disease (CHD). We sought to assess the influence of the genetic defect and the cardiovascular risk factors on the manifestation of atherosclerotic complications in two form
- PMID 25126774
- A neonate with a 'milky' blood. What can it be?
- Bordugo A1, Carlin E1, Demarini S2, Faletra F3, Colonna F1.
- Archives of disease in childhood. Fetal and neonatal edition.Arch Dis Child Fetal Neonatal Ed.2014 Nov;99(6):F514. doi: 10.1136/archdischild-2014-305940. Epub 2014 Apr 19.
- PMID 24747307
Japanese Journal
- LDL-apheresisのリポ蛋白除去に対するリポ蛋白脂質構成の影響:IIa型およびV型高リポ蛋白血症に対する検討
- 伊藤 博夫,石井 寿美,街 稔,武田 佳代子,中村 一路,長瀬 光昌,川村 光信,内藤 周幸
- 日本透析療法学会雑誌 22(3), 337-342, 1989
- … 好ましいと思われた.一方, DSCを用いたLDL-apheresisにより, FH患者では黄色腫, アキレス腱厚の退縮や負荷心電図所見の改善がみられ, V型高リポ蛋白血症患者ではカイロマイクロン血症症候群による腹痛発作の消失が認められた.以上の成績より, DSCへのリポ蛋白吸着は脂質構成にはほとんど影響されないことが示唆され, DSCを用いたLDL-apheresisはIIa型のみならず, IV型やV型の高リポ蛋白血症にも有効である可能性が示唆された. …
- NAID 130003874125
- 加古 博幸,栃原 敏彦,平田 信,原 豊,藤岡 考之,水野 学,岸 均,加藤 伸,八杉 忠男
- 動脈硬化 14(5), 1151-1154, 1986
- … As hypercholesterolemic subjects, familial hypercholesterolemia were studied. … All hyperlipoproteinemic subjects were classified into type IIa, IIb and IV. … In the type ha hyperlipoproteinemia, VLDL has more amounts of cholesterol esters and HDL contains more amounts of free cholesterol than those in the control subjects. …
- NAID 130004883523
- A kindred of familial combined hyperlipidemia (FCHL) with proband showing type V hyperlipoproteinemia.
- KOBORI Shozo,MAEDA Hideo,MIYATA Takao,TAKEDA Haruo,NAKAMURA Nobuhisa,UZAWA Haruo
- Japanese Journal of Medicine 25(3), 306-312, 1986
- … A case of familial hyperlipidemia incidentally found through a 16 year-old high school girl with type V hyperlipoproteinemia and abdominal bouts consistent with this type of hyperlipemia is reported for the first time in Japan. … The laboratory findings of the plasma of her father revealed typical hyperlipoproteinemia of type IIa. …
- NAID 130003513980
★リンクテーブル★
[★]
- 英
- familial hyperlipoproteinemia type IV
- 同
- 家族性高トリグリセリド血症 familial hypertriglyceridemia
- 関
- 高リポ蛋白血症
[★]
- (windows)ファイル内容表示(linux -> cat])
- ex. type report_20111118.jp.htm | php a.php > report_20111118.jp.jp.jp.html
- 関
- form、mode、pattern、type specimen、typed
[★]
[★]
- 関
- family、family member、household、kindred
[★]
- 関
- i.v.、intravascular、intravenous、intravenously
[★]
- 関
- form、mode、pattern、type