Heterotaxy syndrome with mixed bronchopulmonary malinosculation: an unusual case report

[1]  S. Prabhu,et al.  Congenital bronchopulmonary vascular malformations, “sequestration” and beyond , 2015, Indian Journal of Radiology and Imaging.

[2]  I. Shiraishi,et al.  Human heterotaxy syndrome – from molecular genetics to clinical features, management, and prognosis – . , 2012, Circulation journal : official journal of the Japanese Circulation Society.

[3]  S. Kim.  Heterotaxy Syndrome , 2011, Korean circulation journal.

[4]  M. Jehangir,et al.  Congenital lobar emphysema associated with polysplenia syndrome , 2010, Annals of Saudi medicine.

[5]  L. Haramati,et al.  Anomalies of visceroatrial situs. , 2009, AJR. American journal of roentgenology.

[6]  A. Yang,et al.  A Systematic Classification of the Congenital Bronchopulmonary Vascular Malformations: Dysmorphogeneses of the Primitive Foregut System and the Primitive Aortic Arch System , 2008, Yonsei medical journal.

[7]  J. Tröger,et al.  Abdominal sonography in the evaluation of heterotaxy in children , 1995, Pediatric Radiology.

[8]  J. Rome,et al.  Diffuse pulmonary arteriovenous malformation in a child with polysplenia syndrome. , 1995, Pediatric pathology & laboratory medicine : journal of the Society for Pediatric Pathology, affiliated with the International Paediatric Pathology Association.