Truncus arteriosus communis with intact ventricular septum.

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Truncus Arteriosus Communis

22. Harrison TR: Harrison's Principles of Internal Medicine, ed 8, edited by Thorn GS. New York, McGraw-Hill, 1977, p 429 23. Hogg GR: Congenital acute lupus erythematosis associated with subendocardial fibroelastosis. Am J Clin Pathol 28: 648, 1957 24. Brigden W, Bywaters EGL, Lassof MH, Ross IP: The heart in systemic lupus erythematosus. Br Heart J 22: 1, 1960 25. Griffith GC, Vural IL: Acute...

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Persistent Truncus Arteriosus With Intact Ventricular Septum: Clinical, Hemodynamic and Short-term Surgical Outcome

INTRODUCTION Truncus arteriosus with intact ventricular septum is a rare and unique variant of persistent truncus arteriosus (PTA) which usually presents with central cyanosis and congestive heart failure in neonate and early infancy. Associated cardiac and non-cardiac anomalies may affect morbidity and mortality of these patients. CASE PRESENTATION We describe clinical presentation, echocard...

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Rare variant of truncus arteriosus with intact ventricular septum and hypoplastic right ventricle.

A three week old girl was admitted to hospital with severe congestive heart failure and cyanosis. Cross sectional and Doppler echocardiography and cardiac catheterisation showed a unique variant of truncus arteriosus with an intact ventricular septum. The trunk rose only from the left ventricle and was associated with a hypoplastic right ventricle with sinusoids to the right coronary artery.

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Repair of truncus arteriosus with intact ventricular septum (Van Praagh type B2) in a neonate.

superior vena cava draining into the left atrium with absent right superior vena cava. Ann Thorac Surg 1971;11:160-4. 4. Quaegebeur J, Kirklin JW, Pacifico AD, Bargeron LM Jr. Surgical experience with unroofed coronary sinus. Ann Thorac Surg 1979;27:418-25. 5. Chiu IS, Hegerty A, Anderson RH, de Leval M. The landmarks to the atrioventricular conduction system in hearts with absence or unroofing...

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Persistent truncus arteriosus communis with microphthalmos, orbital cyst and polydactyly.

A white woman, aged seventeen, was admitted to hospital in labour. Since the onset of menstruation at fifteen years only six or seven periods had occurred, and the last period could not be accurately dated. The personal and family history was uneventful. A female child was delivered by forceps after a lengthy first stage and cried spontaneously; she was apparently well nourished, was 30 cm. lon...

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ژورنال

عنوان ژورنال: Heart

سال: 1979

ISSN: 1355-6037

DOI: 10.1136/hrt.42.1.97