CASE REPORT
Year : 2016 | Volume
: 17 | Issue : 1 | Page : 27--29
Holt-Oram syndrome associated with aortic atresia: A rare association
Sunil B Rodagi, Snehal S Surana, Vijaykumar R Potdar, Sharanbasav S Kirdi
Department of Paediatrics, Krishna Institute of Medical Sciences, Malkapur, Karad, Maharashtra, India
Correspondence Address:
Sunil B Rodagi
Department of Pediatrics, BLDES SHRI B. M. Patil Medical College, Bijapur - 586103
India
Holt-Oram syndrome (HOS) is a rare autosomal dominant disorder that causes abnormalities of the upper limbs and heart. It is seen in 1:1, 00, 000 live births. It is linked to a single-gene TBX5 “protein-producing” mutation with gene map locus 12q24. Most commonly it is characterized by the cardiac septation defects and pre-axial radial ray abnormalities. We are reporting a case of HOS with aortic atresia which is a rare association.
How to cite this article:
Rodagi SB, Surana SS, Potdar VR, Kirdi SS. Holt-Oram syndrome associated with aortic atresia: A rare association.Heart Views 2016;17:27-29
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How to cite this URL:
Rodagi SB, Surana SS, Potdar VR, Kirdi SS. Holt-Oram syndrome associated with aortic atresia: A rare association. Heart Views [serial online] 2016 [cited 2023 May 30 ];17:27-29
Available from: https://www.heartviews.org/article.asp?issn=1995-705X;year=2016;volume=17;issue=1;spage=27;epage=29;aulast=Rodagi;type=0 |
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