KEGG   DISEASE: 異所性灰白質
エントリ  
H02785                                                             
名称    
異所性灰白質
  上位グループ
神経細胞移動異常症 [DS:H01835]
概要    
Band heterotopia (BH) is a brain malformation caused by a failed migration of cortical neurons during development. Clinical symptoms vary in severity of intellectual disability and may be associated with epileptic disorders. It has been reported that mutations in EML1 cause this disease. The EML1 protein is a member of the microtubule-associated proteins family, playing an important role in microtubule assembly and stabilization as well as in mitotic spindle formation in interphase.
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
   LD20  主な特徴として中枢神経系の異常を伴う症候群
    H02785  異所性灰白質
病因遺伝子 
EML1 [HSA:2009] [KO:K18595]
リンク   
ICD-11: LD20.Y
MeSH: D054221
OMIM: 600348
文献    
  著者
Kielar M, Tuy FP, Bizzotto S, Lebrand C, de Juan Romero C, Poirier K, Oegema R, Mancini GM, Bahi-Buisson N, Olaso R, Le Moing AG, Boutourlinsky K, Boucher D, Carpentier W, Berquin P, Deleuze JF, Belvindrah R, Borrell V, Welker E, Chelly J, Croquelois A, Francis F
  タイトル
Mutations in Eml1 lead to ectopic progenitors and neuronal heterotopia in mouse and human.
  雑誌
Nat Neurosci 17:923-33 (2014)
DOI:10.1038/nn.3729
文献    
  著者
Shaheen R, Sebai MA, Patel N, Ewida N, Kurdi W, Altweijri I, Sogaty S, Almardawi E, Seidahmed MZ, Alnemri A, Madirevula S, Ibrahim N, Abdulwahab F, Hashem M, Al-Sheddi T, Alomar R, Alobeid E, Sallout B, AlBaqawi B, AlAali W, Ajaji N, Lesmana H, Hopkin RJ, Dupuis L, Mendoza-Londono R, Al Rukban H, Yoon G, Faqeih E, Alkuraya FS
  タイトル
The genetic landscape of familial congenital hydrocephalus.
  雑誌
Ann Neurol 81:890-897 (2017)
DOI:10.1002/ana.24964
文献    
  著者
Markus F, Kannengiesser A, Nader P, Atigbire P, Scholten A, Vossing C, Bultmann E, Korenke GC, Owczarek-Lipska M, Neidhardt J
  タイトル
A novel missense variant in the EML1 gene associated with bilateral ribbon-like subcortical heterotopia leads to ciliary defects.
  雑誌
J Hum Genet 66:1159-1167 (2021)
DOI:10.1038/s10038-021-00947-5
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