KEGG   DISEASE: 常染色体優性新生血管炎症性硝子体網膜症
エントリ  
H01798                                                             
名称    
常染色体優性新生血管炎症性硝子体網膜症
概要    
Autosomal dominant neovascular inflammatory vitreoretinopathy (ADNIV) is an inherited autoimmune uveitis and vitreoretinal degeneration characterized by inflammatory cells in the vitreous and anterior chamber, photoreceptor degeneration, vitreous hemorrhages, epiretinal membranes (ERMs), and proliferative iris and retinal neovascularization. It is caused by mutations in CAPN5 gene, encoding an intracellular protease expressed in the retina. In most patients the diagnosis is difficult to make before age 40. Electroretinography can help make the diagnosis in younger individuals in whom the only other sign is the presence of vitreous cells.
カテゴリ  
神経系疾患
階層分類  
ICD-11 による疾患分類 [BR:jp08403]
 09 視覚系の疾患
  眼球後極部の疾患
   網膜の疾患
    9B78  明示された網膜の疾患
     H01798  常染色体優性新生血管炎症性硝子体網膜症
病因遺伝子 
CAPN5 [HSA:726] [KO:K08574]
リンク   
ICD-11: 9B78.2
MeSH: D018630
OMIM: 193235
文献    
  著者
Cham A, Bansal M, Banda HK, Kwon Y, Tlucek PS, Bassuk AG, Tsang SH, Sobol WM, Folk JC, Yeh S, Mahajan VB
  タイトル
Secondary glaucoma in CAPN5-associated neovascular inflammatory vitreoretinopathy.
  雑誌
Clin Ophthalmol 10:1187-97 (2016)
DOI:10.2147/OPTH.S103324
文献    
PMID:1284594
  著者
Stone EM, Kimura AE, Folk JC, Bennett SR, Nichols BE, Streb LM, Sheffield VC
  タイトル
Genetic linkage of autosomal dominant neovascular inflammatory vitreoretinopathy to chromosome 11q13.
  雑誌
Hum Mol Genet 1:685-9 (1992)
DOI:10.1093/hmg/1.9.685
文献    
  著者
Mahajan VB, Skeie JM, Bassuk AG, Fingert JH, Braun TA, Daggett HT, Folk JC, Sheffield VC, Stone EM
  タイトル
Calpain-5 mutations cause autoimmune uveitis, retinal neovascularization, and photoreceptor degeneration.
  雑誌
PLoS Genet 8:e1003001 (2012)
DOI:10.1371/journal.pgen.1003001
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