Heterotaxy Syndrome in A Preterm Baby-A Rare Case Report with Review of Literature  

Sunilkumar M.N. , Parvathy V.K.
Department of Pediatrics, Amala Institute of Medical Sciences, Amala Nagar, Thrissur-680 555, Kerala, India
Author    Correspondence author
International Journal of Clinical Case Reports, 2015, Vol. 5, No. 41   doi: 10.5376/ijccr.2015.05.0041
Received: 26 Apr., 2015    Accepted: 17 Jun., 2015    Published: 26 Oct., 2015
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This is an open access article published under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Preferred citation for this article:

Sunilkumar M.N. and Parvathy V.K., 2015, Heterotaxy Syndrome in A Preterm Baby-A Rare Case Report with  Review of Literature, International Journal of Clinical Case Reports, 5(41) 1-5 (doi: 10.5376/ijccr.2015.05.0041)

Abstract

Heterotaxy syndrome (HTS) is an abnormality where the internal thoraco-abdominal organs are arranged abnormally across the left-right axis of the body. Literature review has reported that it is a very rare condition and has complex cardiac and extracardiac manifestations which requires early surgical intervention. A very rare case report of HTS in a preterm newborn with  an associated  duodenal atresia is presented with a review of literature.

Keywords
Heterotaxy; Heterotaxy syndrome; Complex cardiac abnormalities; Duodenal atresia; Palliative surgery
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