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A rare cause of cardiomyopathy in an infant: middle aortic syndrome

Published online by Cambridge University Press:  14 November 2016

Arshid Mir ,
Benjamin Stam  and
Charles Sperrazza
Arshid Mir*
Affiliation:
Department of Pediatrics, Division of Pediatric Cardiology, Oklahoma University Health Sciences Center, Oklahoma City, Oklahoma, United States of America
Benjamin Stam
Affiliation:
Department of Anesthesiology, University of Michigan, Ann Arbor, Michigan, United States of America
Charles Sperrazza
Affiliation:
Department of Pediatrics, Division of Pediatric Cardiology, Oklahoma University Health Sciences Center, Oklahoma City, Oklahoma, United States of America
*
Correspondence to: A. Mir, MD, Department of Pediatrics, Division of Pediatric Cardiology, Oklahoma University Health Sciences Center, Oklahoma City, OK 73014, United States of America. Tel: 405 271 4411 ext. 44406; E-mail: arshid-mir@ouhsc.edu
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Abstract

Coarctation of the abdominal aorta is a rare condition with a handful of cases reported in infancy. We report the case of a 4-month-old infant with severe abdominal coarctation who presented with dilated cardiomyopathy. Following successful transcatheter-based stenting of her abdominal aorta, her cardiomyopathy resolved.

Keywords

Cardiomyopathymid-aortic syndromestent placement
Type
Brief Report
Information
Cardiology in the Young , Volume 27 , Issue 4 , May 2017 , pp. 794 - 796
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Copyright
© Cambridge University Press 2016 

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References

1. Daghero, F, Bueno, N, Peirone, A, Ochoa, J, Fao Torres, G, Ganame, J. Coarctation of the abdominal aorta: an uncommon cause of arterial hypertension and stroke. Circ Cardiovasc Imaging 2008; 1: e4–e6.Google Scholar
2. Das, BB, Recto, M, Shoemaker, L, Mitchell, M, Austin, EH. Midaortic syndrome presenting as neonatal hypertension. Pediatr Cardiol 2008; 29: 1000–1001.Google Scholar
3. Parent, JJ, Bendaly, EA, Hurwitz, RA. Abdominal coarctation and associated comorbidities in children. Congenit Heart Dis 2014; 9: 69–74.Google Scholar
4. Zeltser, I, Parness, IA, Ko, H, Holzman, IR, Kamenir, SA. Midaortic syndrome in the fetus and premature newborn: a new etiology of nonimmune hydrops fetalis and reversible fetal cardiomyopathy. Pediatrics 2003 Jun; 111 (Pt 1): 1437–1442.Google Scholar
5. Sethna, CB, Kaplan, BS, Cahill, AM, Velazquez, OC, Meyers, KE. Idiopathic mid-aortic syndrome in children. Pediatr Nephrol 2008; 23: 1135–1142.CrossRefGoogle ScholarPubMed
6. Tummolo, A, Marks, SD, Stadermann, M, et al. Mid-aortic syndrome: long-term outcome of 36 children. Pediatr Nephrol 2009; 24: 2225–2232.CrossRefGoogle ScholarPubMed
7. Pilati, M, Pongiglione, G, Gagliardi, MG. Percutaneous treatment of abdominal coarctation in children using a covered stent. Pediatr Cardiol 2013; 34: 2080–2085.Google Scholar