KEGG   DISEASE: CEDNIK 症候群
エントリ  
H00799                                                             
名称    
CEDNIK 症候群
概要    
CEDNIK (Cerebral dysgenesis, neuropathy, ichthyosis and keratoderma) syndrome is a rare condition that shows severe developmental failure of the nervous system and the epidermis. Clinical manifestations include microcephaly, cerebral dysgenesis, facial dysmorphism, palmoplantar keratoderma, and ichthyosis. Decreased expression of SNAP29, a member of the SNARE family of proteins, is linked to abnormal lamellar granule maturation and abnormal epidermal differentiation.
カテゴリ  
先天奇形
階層分類  
ICD-11 による疾患分類 [BR:jp08403]
 20 発達異常
  多発性の発達異常または症候群
   LD27  主な特徴として皮膚または粘膜の異常を伴う症候群
    H00799  CEDNIK 症候群
パスウェイに基づく疾患分類 [BR:jp08402]
 細胞プロセス
  nt06532  オートファジー
   H00799  CEDNIK 症候群
パスウェイ 
hsa04140  Autophagy - animal
hsa04130  SNARE interactions in vesicular transport
ネットワーク
nt06532 Autophagy
病因遺伝子 
SNAP29 [HSA:9342] [KO:K08509]
リンク   
ICD-11: LD27.2
MeSH: C537943
OMIM: 609528
文献    
  著者
Sprecher E, Ishida-Yamamoto A, Mizrahi-Koren M, Rapaport D, Goldsher D, Indelman M, Topaz O, Chefetz I, Keren H, O'brien TJ, Bercovich D, Shalev S, Geiger D, Bergman R, Horowitz M, Mandel H
  タイトル
A mutation in SNAP29, coding for a SNARE protein involved in intracellular trafficking, causes a novel neurocutaneous syndrome characterized by cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma.
  雑誌
Am J Hum Genet 77:242-51 (2005)
DOI:10.1086/432556
文献    
  著者
Fuchs-Telem D, Stewart H, Rapaport D, Nousbeck J, Gat A, Gini M, Lugassy Y, Emmert S, Eckl K, Hennies HC, Sarig O, Goldsher D, Meilik B, Ishida-Yamamoto A, Horowitz M, Sprecher E
  タイトル
CEDNIK syndrome results from loss-of-function mutations in SNAP29.
  雑誌
Br J Dermatol 164:610-6 (2011)
DOI:10.1111/j.1365-2133.2010.10133.x
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