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
- a disorder (usually of unknown origin) of the heart muscle (myocardium) (同)myocardiopathy
PrepTutorEJDIC
- 家族の,家族特有の / 違伝的な,血統にあらわれる
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.
- 1. 肥大型心筋症の遺伝学 genetics of hypertrophic cardiomyopathy
- 2. 肥大型心筋症の自然経過 natural history of hypertrophic cardiomyopathy
- 3. 肥大型心筋症における内科的治療 medical therapy in hypertrophic cardiomyopathy
- 4. 閉塞性肥大型心筋症の種類および病態生理 types and pathophysiology of obstructive hypertrophic cardiomyopathy
- 5. 特殊な問題の治療を含む肥大型心筋症のマネージメントの概要 overview of hypertrophic cardiomyopathy management including treatment of special problems
English Journal
- Genetics of sudden cardiac death.
- Refaat MM1, Hotait M, London B.
- Current cardiology reports.Curr Cardiol Rep.2015 Jul;17(7):606. doi: 10.1007/s11886-015-0606-8.
- Sudden cardiac death (SCD) is defined by the World Health Organization (WHO) as death within 1 h of symptom onset (witnessed) or within 24 h of being observed alive and symptom free (unwitnessed). It affects more than 3 million people annually worldwide and affects approximately 1/1000 people eac
- PMID 26026997
- Compound heterozygous or homozygous truncating MYBPC3 mutations cause lethal cardiomyopathy with features of noncompaction and septal defects.
- Wessels MW1, Herkert JC2, Frohn-Mulder IM3, Dalinghaus M3, van den Wijngaard A4, de Krijger RR5, Michels M6, de Coo IF7, Hoedemaekers YM2, Dooijes D8.
- European journal of human genetics : EJHG.Eur J Hum Genet.2015 Jul;23(7):922-8. doi: 10.1038/ejhg.2014.211. Epub 2014 Oct 22.
- Familial hypertrophic cardiomyopathy (HCM) is usually caused by autosomal dominant pathogenic mutations in genes encoding sarcomeric or sarcomere-associated cardiac muscle proteins. The disease mainly affects adults, although young children with severe HCM have also been reported. We describe four u
- PMID 25335496
Japanese Journal
- Prevalence and Distribution of Sarcomeric Gene Mutations in Japanese Patients With Familial Hypertrophic Cardiomyopathy
- OTSUKA Haruna,ARIMURA Takuro,ABE Tadaaki,KAWAI Hiroya,AIZAWA Yoshiyasu,KUBO Toru,KITAOKA Hiroaki,NAKAMURA Hiroshi,NAKAMURA Kazufumi,OKAMOTO Hiroshi,ICHIDA Fukiko,AYUSAWA Mamoru,NUNODA Shinichi,ISOBE Mitsuaki,MATSUZAKI Masunori,DOI Yoshinori L.,FUKUDA Keiichi,SASAOKA Taishi,IZUMI Toru,ASHIZAWA Naoto,KIMURA Akinori
- Circulation journal : official journal of the Japanese Circulation Society 76(2), 453-461, 2012-01-25
- … Hypertrophic cardiomyopathy (HCM), which is inherited as an autosomal dominant trait, is the most prevalent hereditary cardiac disease. … MYBPC3</i>, <i>MYL2</i>, <i>MYL3</i>, <i>TNNT2</i>, <i>TNNI3</i>, <i>TPM1</i>, and <i>ACTC</i>, was performed by direct sequencing in 112 unrelated Japanese proband patients with familial HCM; …
- NAID 10030035969
- Multicenter Study of the Prevalence and Distribution of Sarcometric Gene Mutations in Familial Hypertrophic Cardiomyopathy : A Milestone for Genetic Diagnosis in the Japanese Population
- NIWANO Shinichi
- Circulation journal : official journal of the Japanese Circulation Society 76(2), 303-304, 2012-01-25
- NAID 10030035335
Related Links
- 17 May 2011 ... Disease characteristics. Hypertrophic cardiomyopathy (HCM), caused by mutation in one of the genes currently known to encode different components of the sarcomere, is characterized by left ventricular hypertrophy (LVH) in ...
Related Pictures
★リンクテーブル★
| リンク元 | 「FHC」「家族性肥大心筋症」「家族性肥大型心筋症」 |
| 関連記事 | 「familial」「hypertrophic」 |
「FHC」
「家族性肥大心筋症」
「家族性肥大型心筋症」
「familial」
- adj.
- 家族性の、家系性の、家族の
「hypertrophic」
- adj.
- 肥大性の、肥大型の、肥厚性の、肥大症の