Literature DB >> 21087434

Anomalous origin of the left coronary artery from the pulmonary artery in Alagille syndrome.

Tara J Lemoine1, Aditya K Kaza, Robert Gray, Ronald W Day, Lloyd Y Tani, William Bradley Poss.   

Abstract

Alagille syndrome is a dominantly inherited multisystem disorder involving multiple organs including the liver, heart, eyes, face, and skeleton. Congenital heart defects, the majority of which are right-sided, contribute significantly to the mortality of these patients. We report a patient with Alagille syndrome who presented with mitral valve regurgitation requiring valvuloplasty and subsequent mitral valve replacement. The patient was ultimately diagnosed with anomalous origin of the left coronary artery from the pulmonary artery and underwent successful reimplantation.

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Year:  2010        PMID: 21087434     DOI: 10.1111/j.1747-0803.2010.00386.x

Source DB:  PubMed          Journal:  Congenit Heart Dis        ISSN: 1747-079X            Impact factor:   2.007


  1 in total

1.  Novel Heterozygous Mutations in JAG1 and NOTCH2 Genes in a Neonatal Patient with Alagille Syndrome.

Authors:  Alisa Brennan; Anil Kesavan
Journal:  Case Rep Pediatr       Date:  2017-03-29
  1 in total

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