KEGG   DISEASE: 非表皮剥離性焦点掌蹠角化症
エントリ  
H02263                                                             
名称    
非表皮剥離性焦点掌蹠角化症
  上位グループ
非表皮剥離性掌蹠角化症 [DS:H00723]
掌蹠角化症 [DS:H01673]
概要    
Focal nonepidermolytic palmoplantar keratoderma (FNEPPK) is a genetically heterogeneous phenotype characterized by the presence, on the palms and soles, of circumscribed calluses. These can be painful. It has been reported that mutations in keratin 16 (KRT16) and TRPV3 gene cause FNEPPK. Both of them are inherited in an autosomal dominant manner.
カテゴリ  
先天奇形
階層分類  
ICD-11 による疾患分類 [BR:jp08403]
 14 皮膚の疾患
  皮膚の遺伝性及び発達性疾患
   EC20  遺伝性角化症
    H02263  非表皮剥離性焦点掌蹠角化症
病因遺伝子 
(FNEPPK1) KRT16 [HSA:3868] [KO:K07604]
(FNEPPK2) TRPV3 [HSA:162514] [KO:K04972]
リンク   
ICD-11: EC20.31
OMIM: 613000 616400
文献    
  著者
He Y, Zeng K, Zhang X, Chen Q, Wu J, Li H, Zhou Y, Glusman G, Roach J, Etheridge A, Qing S, Tian Q, Lee I, Tian X, Wang X, Wu Z, Hood L, Ding Y, Wang K
  タイトル
A gain-of-function mutation in TRPV3 causes focal palmoplantar keratoderma in a Chinese family.
  雑誌
J Invest Dermatol 135:907-909 (2015)
DOI:10.1038/jid.2014.429
文献    
  著者
Smith FJ, Fisher MP, Healy E, Rees JL, Bonifas JM, Epstein EH Jr, Tan EM, Uitto J, McLean WH
  タイトル
Novel keratin 16 mutations and protein expression studies in pachyonychia congenita type 1 and focal palmoplantar keratoderma.
  雑誌
Exp Dermatol 9:170-7 (2000)
DOI:10.1034/j.1600-0625.2000.009003170.x
文献    
PMID:8595410
  著者
Shamsher MK, Navsaria HA, Stevens HP, Ratnavel RC, Purkis PE, Kelsell DP, McLean WH, Cook LJ, Griffiths WA, Gschmeissner S, et al.
  タイトル
Novel mutations in keratin 16 gene underly focal non-epidermolytic palmoplantar keratoderma (NEPPK) in two families.
  雑誌
Hum Mol Genet 4:1875-81 (1995)
DOI:10.1093/hmg/4.10.1875
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