KEGG   DISEASE: 好中球減少を伴う多形皮膚萎縮症
エントリ  
H00793                                                             
名称    
好中球減少を伴う多形皮膚萎縮症
概要    
Poikiloderma with neutropenia is an inherited genodermatosis found in Navajo people. It is characterized by erythematous rash that appears in the first year of life. The rash starts from the limbs and spreads to the trunk and the face, evolving into poikiloderma. Patients with this disease have recurrent bacterial infections and chronic neutropenia. It has been reported mutations in USB1 cause this condition.
カテゴリ  
皮膚疾患
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
   皮膚の遺伝性症候群
    EC10  多形皮膚萎縮症を伴う遺伝性症候群
     H00793  好中球減少を伴う多形皮膚萎縮症
病因遺伝子 
USB1 [HSA:79650] [KO:K23093]
コメント  
Dyskeratosis congenita (H00507) and Rothmund-Thomson syndrome (H00296) display clinical overlap with this disease.
リンク   
ICD-11: EC10
MeSH: C565820
OMIM: 604173
文献    
  著者
Chantorn R, Shwayder T
  タイトル
Poikiloderma with neutropenia: report of three cases including one with calcinosis cutis.
  雑誌
Pediatr Dermatol 29:463-72 (2012)
DOI:10.1111/j.1525-1470.2011.01513.x
文献    
  著者
Arnold AW, Itin PH, Pigors M, Kohlhase J, Bruckner-Tuderman L, Has C
  タイトル
Poikiloderma with neutropenia: a novel C16orf57 mutation and clinical diagnostic criteria.
  雑誌
Br J Dermatol 163:866-9 (2010)
DOI:10.1111/j.1365-2133.2010.09929.x
文献    
  著者
Walne AJ, Vulliamy T, Beswick R, Kirwan M, Dokal I
  タイトル
Mutations in C16orf57 and normal-length telomeres unify a subset of patients with dyskeratosis congenita, poikiloderma with neutropenia and Rothmund-Thomson syndrome.
  雑誌
Hum Mol Genet 19:4453-61 (2010)
DOI:10.1093/hmg/ddq371
文献    
  著者
Van Hove JL, Jaeken J, Proesmans M, Boeck KD, Minner K, Matthijs G, Verbeken E, Demunter A, Boogaerts M
  タイトル
Clericuzio type poikiloderma with neutropenia is distinct from Rothmund-Thomson syndrome.
  雑誌
Am J Med Genet A 132A:152-8 (2005)
DOI:10.1002/ajmg.a.30430
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