Aortic stenosis in hypoplastic right heart syndrome, associated with interstitial deletion of chromosome 2

J. Sharma, D. Friedman, Myles S. Schiller, P. Flynn, M. L. Alonso

Research output: Contribution to journalArticle

7 Citations (Scopus)

Abstract

This report describes a rare case of moderate to severe valvular aortic stenosis in the setting of severe tricuspid stenosis, pulmonary atresia with intact interventricular septum and right ventricular dependent coronary circulation. We discuss the clinical, hemodynamic, echocardiographic and angiocardiographic findings on this rare case and comment on accompanied malformations, with its possible association observed to the interstitial deletion of band q22 or q24 of the long arm of chromosome 2.

Original languageEnglish (US)
Pages (from-to)199-202
Number of pages4
JournalInternational Journal of Cardiology
Volume62
Issue number3
DOIs
StatePublished - Dec 19 1997
Externally publishedYes

Fingerprint

Pulmonary Atresia
Ventricular Septum
Coronary Circulation
Chromosomes, Human, Pair 2
Aortic Valve Stenosis
Pathologic Constriction
Hemodynamics

Keywords

  • Agenesis of corpus callosum
  • Aortic stenosis
  • Hypoplastic right heart syndrome
  • Interstitial 2q deletion
  • Pulmonary atresia

ASJC Scopus subject areas

  • Cardiology and Cardiovascular Medicine

Cite this

Aortic stenosis in hypoplastic right heart syndrome, associated with interstitial deletion of chromosome 2. / Sharma, J.; Friedman, D.; Schiller, Myles S.; Flynn, P.; Alonso, M. L.

In: International Journal of Cardiology, Vol. 62, No. 3, 19.12.1997, p. 199-202.

Research output: Contribution to journalArticle

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