KEGG   DISEASE: 間脳・中脳接合部異形成症候群
エントリ  
H02487                                                             
名称    
間脳・中脳接合部異形成症候群
概要    
Diencephalic-mesencephalic junction dysplasia syndrome (DMJDS) is a novel autosomal recessive brain malformation. DMJDS is associated with a characteristic butterfly-shaped contour of the midbrain on axial sections on MRI. Patients displayed severe cognitive impairment, post-natal progressive microcephaly, axial hypotonia, spastic quadriparesis and seizures. A few genes that cause DMJDS have been identified.
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
    H02487  間脳・中脳接合部異形成症候群
病因遺伝子 
(DMJDS1) PCDH12 [HSA:51294] [KO:K16499]
(DMJDS2) GSX2 [HSA:170825] [KO:K09310]
リンク   
ICD-11: LD20.Y
OMIM: 251280 618646
文献    
  著者
Zaki MS, Saleem SN, Dobyns WB, Barkovich AJ, Bartsch H, Dale AM, Ashtari M, Akizu N, Gleeson JG, Grijalvo-Perez AM
  タイトル
Diencephalic-mesencephalic junction dysplasia: a novel recessive brain malformation.
  雑誌
Brain 135:2416-27 (2012)
DOI:10.1093/brain/aws162
文献    
  著者
De Mori R, Severino M, Mancardi MM, Anello D, Tardivo S, Biagini T, Capra V, Casella A, Cereda C, Copeland BR, Gagliardi S, Gamucci A, Ginevrino M, Illi B, Lorefice E, Musaev D, Stanley V, Micalizzi A, Gleeson JG, Mazza T, Rossi A, Valente EM
  タイトル
Agenesis of the putamen and globus pallidus caused by recessive mutations in the homeobox gene GSX2.
  雑誌
Brain 142:2965-2978 (2019)
DOI:10.1093/brain/awz247
LinkDB    

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