KEGG   DISEASE: エドワ−ズ症候群
エントリ  
H01564                                                             
名称    
エドワ−ズ症候群;
18 トリソミー
概要    
Edwards syndrome, also known as trisomy 18, is a chromosomal disorder due to the presence of an extra chromosome 18, either full, mosaic trisomy, or partial trisomy 18q. This disease is the second-most common autosomal trisomy, after Down syndrome. The live born prevalence is estimated as 1/6,000-1/8,000, but the overall prevalence is higher (1/2500-1/2600) due to the high frequency of fetal loss and pregnancy termination after prenatal diagnosis. The main clinical features include prenatal growth deficiency, characteristic craniofacial features, distinctive hand posture, nail hypoplasia, short hallux, short sternum, and major malformations (particularly involving the heart). Approximately 50% of newborns survive beyond 1 week while more than 90% do not survive beyond 1 years of age.
カテゴリ  
染色体異常
階層分類  
ICD-11 による疾患分類 [BR:jp08403]
 20 発達異常
  遺伝子変異を除く染色体異常
   LD40  常染色体の完全なトリソミー
    H01564  エドワ−ズ症候群
リンク   
ICD-11: LD40.2
MeSH: C580500
文献    
  著者
Imataka G, Suzumura H, Arisaka O
  タイトル
Clinical features and survival in individuals with trisomy 18: A retrospective one-center study of 44 patients who received intensive care treatments.
  雑誌
Mol Med Rep 13:2457-66 (2016)
DOI:10.3892/mmr.2016.4806
文献    
  著者
Cereda A, Carey JC
  タイトル
The trisomy 18 syndrome.
  雑誌
Orphanet J Rare Dis 7:81 (2012)
DOI:10.1186/1750-1172-7-81
文献    
  著者
Zhang H, Gao Y, Jiang F, Fu M, Yuan Y, Guo Y, Zhu Z, Lin M, Liu Q, Tian Z, Zhang H, Chen F, Lau TK, Zhao L, Yi X, Yin Y, Wang W
  タイトル
Non-invasive prenatal testing for trisomies 21, 18 and 13: clinical experience from 146,958 pregnancies.
  雑誌
Ultrasound Obstet Gynecol 45:530-8 (2015)
DOI:10.1002/uog.14792
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