KEGG   DISEASE: 肢帯型筋ジストロフィー 2B
エントリ  
H01974                                                             
名称    
肢帯型筋ジストロフィー 2B
概要    
Limb-girdle muscular dystrophy type 2B (LGMD2B) is an autosomal recessive phenotype of dysferlinopathies, muscle disorders caused by mutations in the dysferlin gene (DYSF). Clinically, it is characterized by weakness in the proximal muscles at onset, involving predominantly the lower limbs. At late stages of the disease, loss of muscle bulk in the pelvic girdle and calf may appear. Onset is typically in the late teens or early adulthood.
カテゴリ  
神経系疾患; 筋骨格疾患
階層分類  
ICD-11 による疾患分類 [BR:jp08403]
 08 神経系の疾患
  神経筋接合部または筋の疾患
   原発性筋疾患
    8C70  筋ジストロフィー
     H01974  肢帯型筋ジストロフィー 2B
病因遺伝子 
DYSF [HSA:8291] [KO:K18261]
リンク   
ICD-11: 8C70.41
MeSH: C535899
OMIM: 253601
文献    
  著者
Szymanska S, Rokicki D, Karkucinska-Wieckowska A, Szymanska-Debinska T, Ciara E, Ploski R, Grajkowska W, Pronicki M
  タイトル
Case report of an adolescent girl with limb-girdle muscular dystrophy type 2B - the usefulness of muscle protein immunostaining in the diagnosis of dysferlinopathies.
  雑誌
Folia Neuropathol 52:452-6 (2014)
DOI:10.5114/fn.2014.47847
文献    
  著者
Illa I, De Luna N, Dominguez-Perles R, Rojas-Garcia R, Paradas C, Palmer J, Marquez C, Gallano P, Gallardo E
  タイトル
Symptomatic dysferlin gene mutation carriers: characterization of two cases.
  雑誌
Neurology 68:1284-9 (2007)
DOI:10.1212/01.wnl.0000256768.79353.60
文献    
  著者
Illarioshkin SN, Ivanova-Smolenskaya IA, Greenberg CR, Nylen E, Sukhorukov VS, Poleshchuk VV, Markova ED, Wrogemann K
  タイトル
Identical dysferlin mutation in limb-girdle muscular dystrophy type 2B and distal myopathy.
  雑誌
Neurology 55:1931-3 (2000)
DOI:10.1212/wnl.55.12.1931
文献    
PMID:8808603
  著者
Weiler T, Greenberg CR, Nylen E, Halliday W, Morgan K, Eggertson D, Wrogemann K
  タイトル
Limb-girdle muscular dystrophy and Miyoshi myopathy in an aboriginal Canadian kindred map to LGMD2B and segregate with the same haplotype.
  雑誌
Am J Hum Genet 59:872-8 (1996)
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