KEGG   DISEASE: 低身長・顔異形・薄毛を伴う成長遅滞
エントリ  
H02368                                                             
名称    
低身長・顔異形・薄毛を伴う成長遅滞
概要    
Developmental delay with short stature, dysmorphic facial features, and sparse hair (DEDSSH) is an autosomal recessive intellectual disability with short stature, craniofacial and ectodermal anomalies. It has been reported that DPH1 is responsible gene for DEDSSH.
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
   LD2F  多発性の構造異常を伴う症候群, 主な体系の関与を伴わないもの
    H02368  低身長・顔異形・薄毛を伴う成長遅滞
病因遺伝子 
(DEDSSH1) DPH1 [HSA:1801] [KO:K07561]
(DEDSSH2) DPH2 [HSA:1802] [KO:K17866]
リンク   
ICD-11: LD2F.1Y
OMIM: 616901 620062
文献    
PMID:26220823 (DPH1)
  著者
Loucks CM, Parboosingh JS, Shaheen R, Bernier FP, McLeod DR, Seidahmed MZ, Puffenberger EG, Ober C, Hegele RA, Boycott KM, Alkuraya FS, Innes AM
  タイトル
Matching two independent cohorts validates DPH1 as a gene responsible for autosomal recessive intellectual disability with short stature, craniofacial, and ectodermal anomalies.
  雑誌
Hum Mutat 36:1015-9 (2015)
DOI:10.1002/humu.22843
文献    
PMID:32576952 (DPH2)
  著者
Hawer H, Mendelsohn BA, Mayer K, Kung A, Malhotra A, Tuupanen S, Schleit J, Brinkmann U, Schaffrath R
  タイトル
Diphthamide-deficiency syndrome: a novel human developmental disorder and ribosomopathy.
  雑誌
Eur J Hum Genet 28:1497-1508 (2020)
DOI:10.1038/s41431-020-0668-y
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