KEGG   DISEASE: 長島型掌蹠角化症
エントリ  
H02264                                                             
名称    
長島型掌蹠角化症
  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    
Palmoplantar keratoderma Nagashima type (PPKN) is an autosomal recessive nonsyndromic diffuse palmoplantar keratosis characterized by diffuse hyperkeratosis with redness, expanding on to the dorsal surfaces of the palms and feet and the Achilles tendon area. Its clinical manifestations are similar to but milder than those of mal de Meleda. It has been reported that mutations in SERPINB7, encoding a member of the serine protease inhibitor, cause PPKN.
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
    H02264  長島型掌蹠角化症
病因遺伝子 
SERPINB7 [HSA:8710] [KO:K13964]
リンク   
ICD-11: EC20.30
ICD-10: Q82.8
OMIM: 615598
文献    
  著者
Kabashima K, Sakabe J, Yamada Y, Tokura Y
  タイトル
"Nagashima-type" keratosis as a novel entity in the palmoplantar keratoderma category.
  雑誌
Arch Dermatol 144:375-9 (2008)
DOI:10.1001/archderm.144.3.375
文献    
  著者
Kubo A, Shiohama A, Sasaki T, Nakabayashi K, Kawasaki H, Atsugi T, Sato S, Shimizu A, Mikami S, Tanizaki H, Uchiyama M, Maeda T, Ito T, Sakabe J, Heike T, Okuyama T, Kosaki R, Kosaki K, Kudoh J, Hata K, Umezawa A, Tokura Y, Ishiko A, Niizeki H, Kabashima K, Mitsuhashi Y, Amagai M
  タイトル
Mutations in SERPINB7, encoding a member of the serine protease inhibitor superfamily, cause Nagashima-type palmoplantar keratosis.
  雑誌
Am J Hum Genet 93:945-56 (2013)
DOI:10.1016/j.ajhg.2013.09.015

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