阿拉吉歐症候群是一種體染色體基因異常的疾病,其會導致膽汁鬱積、先天性心臟血管疾病、骨骼結構異常、眼球角膜異常以及特殊的外觀長相。此病通常藉由肝臟內膽管的數目來判定。
其發生率為1/70000,但數字有可能被低估。
遺傳方面,其遺傳方式為體染色體顯性遺傳疾病。
參考資料
*[http://www.genes-at-taiwan.com.tw/genehelp/ 罕見遺傳疾病一點通]
外部連結
- [http://www.alagille.org Official Website for the Alagille Syndrome Alliance]
- [https://web.archive.org/web/20111110075804/http://www.agsbulletinboard.info/forums/index.php Official Alagille Syndrome Alliance message board]
- [http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=alagille GeneReviews/NCBI/UW/NIH entry on Alagille syndrome]
- [http://www.ncbi.nlm.nih.gov/omim/118450,600275,601920,610205,118450,600275,601920,610205 OMIM entries on Alagille syndrome]
*[http://www.cincinnatichildrens.org/svc/alpha/l/liver/diseases/alagille-syndrome.htm Alagille Syndrome, Liver Diseases and Treatments, Cincinnati Children's Hospital Medical Center]
*[http://archive.wikiwix.com/cache/20130123232854/http://alagille.org/data/medical.pdf Information] from the Alagille Syndrome Alliance
- [http://www.childliverdisease.org Children's Liver Disease Foundation]
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