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Infundibular Pulmonary Stenosis

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Experience with balloon pulmonary valvuloplasty and predictors of outcome: a ten-year study.

Sonia A El-Saeidi, Hala S Hamza, Hala M Agha, Mohammed M Soliman, Wael A Attia, Rania El-Kaffas, Faten Abdel-Aziz, Osama Abdel-Aziz, Sahar Shaker, Amira Esmat, Rasha Ammar, Aya Fattouh, Khalid Mohi-Eldin, Amal M El-Sisi,

BACKGROUND:Balloon pulmonary valvuloplasty is the treatment of choice for patients with moderate to severe pulmonary valve stenosis. METHODS:An observational retrospective cross-sectional study including neonates, small infants, and children who underwent balloon pulmonary valvuloplasty in the period from 2007 to 2016 in the cardiac catheterisation unit of the paediatric cardiology department ... Read more >>

Cardiol Young (Cardiology in the young)
[2020, :1-7]

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Multi-detector computed tomography angiographic evaluation of right ventricular outflow tract obstruction and other associated cardiovascular anomalies in tetralogy of Fallot patients.

Rani Kunti R Singh, Neeraj Jain, Sunil Kumar, Naveen Garg,

Purpose:To evaluate various types of right ventricular outflow tract obstruction associated with tetralogy of Fallot (TOF) with emphasis on the abnormality of pulmonary arterial system and other associated cardiovascular anomalies using computed tomography (CT) angiography. Material and methods:We retrospectively evaluated 184 consecutive previously diagnosed TOF patients who underwent CT angiography ... Read more >>

Pol J Radiol (Polish journal of radiology)
[2019, 84:e511-e516]

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Prevalence and management of coronary artery anomalies in tetralogy of Fallot at Cheikh Zaid Hospital's Pediatric Cardiac Surgery Department in Morocco: retrospective study.

Mohamed Rida Ajaja, Amine Cheikh, Hicham Rhazali, Mustapha Bouatia, Anas Slaoui, Redouane Abouqal, Amine El Hassani, Younes Cheikhaoui,

Introduction:Tetralogy of Fallot (TOF) is one of the most common cyanogenic congenital heart defects. It represents 10% of congenital heart diseases in children. Coronary artery anomalies (CAA) have been reported in 2% to 14% of cases in patients with TOF, according to angiographic, surgical and autopsy series. Many of these ... Read more >>

Pan Afr Med J (The Pan African medical journal)
[2019, 34:157]

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Cardiofacial Syndrome: A Rare Case Report.

S A Sunny, S I Alam, A B Adhikary, M A Hossain,

Cardiofacial syndrome is associated with facial abnormality with congenital heart disease. Here, we report a case of cardiofacial syndrome having anotia and facial nerve palsy on the right side in combination with infundibular pulmonary stenosis and patent ductus arteriosus which is a rare presentation of cardiofacial syndrome. A 6 years ... Read more >>

Mymensingh Med J (Mymensingh medical journal : MMJ)
[2019, 28(4):945-948]

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Extrapulmonic presentation of tuberculosis: An atypical urogenital presentation of a common disease.

Matthew Pagni, Matthew Thompson, Kacy Ramirez, George Koberlein,

Mycobacterium tuberculosis is the leading cause of infectious disease-related death worldwide. However, it is less frequently encountered in developed countries, and 90% of cases are reported in adults, making it a less commonly encountered entity in pediatric radiology. The disease is treatable, but symptoms of renal disease are nonspecific and ... Read more >>

Radiol Case Rep (Radiology case reports)
[2020, 15(5):596-601]

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Congenital supravalvular and subvalvular pulmonary stenosis with hypoplastic pulmonary annulus associated with congenital rubella syndrome.

Dibbendhu Khanra, Yash Shrivastava, Bhanu Duggal, Shishir Soni,

BMJ Case Rep (BMJ case reports)
[2019, 12(7):]

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Complete sternal cleft with tetralogy of Fallot.

Debasis Das, Nilanjan Dutta, Pratik Pandey, Adhish Basu, Manish Kumar Sharma, Rangan Koley, Amitabha Chattopadhyay,

Complete sternal cleft is a very rare congenital midline defect of the sternum. It is not uncommonly associated with intracardiac defects. We report a case of a 2-year-old child with complete sternal cleft and tetralogy of Fallot who presented with cyanotic spells. The child underwent total correction, followed by chest ... Read more >>

Ann Pediatr Cardiol (Annals of pediatric cardiology)
[2020, 13(1):81-83]

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Surgical Treatment of Infective Endocarditis in Pulmonary Position-15 Years Single Centre Experience.

Daina Liekiene, Laurynas Bezuska, Palmyra Semeniene, Rasa Cypiene, Virgilijus Lebetkevicius, Virgilijus Tarutis, Jurate Barysiene, Kestutis Rucinskas, Vytautas Sirvydis,

Background and Objectives: Infective endocarditis in the pulmonary position is a rare disease. Isolated pulmonary valve endocarditis is extremely rare. The aim of our study was to assess patients who were treated surgically for pulmonary endocarditis at our institution from January 2003 to December 2017. Materials and Methods: We analyze ... Read more >>

Medicina (Kaunas) (Medicina (Kaunas, Lithuania))
[2019, 55(9):]

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Case 3/2019 - Type IIB Tricuspid Atresia, in Natural Evolution, at 21 Years of Age.

Edmar Atik, Alessandra Costa Barreto, Maria Angélica Binotto,

Arq. Bras. Cardiol. (Arquivos brasileiros de cardiologia)
[2019, 112(5):592-593]

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The Rare Association of Tetralogy of Fallot and ALCAPA.

Alexandre Noboru Murakami, Gabriela Guimarães Baston, Mariana Ribeiro Rodero Cardoso, Carlos Henrique de Marchi, Ulisses Alexandre Croti,

Braz J Cardiovasc Surg (Brazilian journal of cardiovascular surgery)
[2019, 34(5):624-626]

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Tetralogy of Fallot: morphological variations and implications for surgical repair.

Saad M Khan, Nigel E Drury, John Stickley, David J Barron, William J Brawn, Timothy J Jones, Robert H Anderson, Adrian Crucean,

OBJECTIVES:Tetralogy of Fallot is characterized by anterocephalad deviation of the outlet septum, along with abnormal septoparietal trabeculations, which lead to subpulmonary infundibular stenosis. Archives of retained hearts are an important resource for improving our understanding of congenital heart defects and their morphological variability. This study aims to define variations in ... Read more >>

Eur J Cardiothorac Surg (European journal of cardio-thoracic surgery : official journal of the European Association for Cardio-thoracic Surgery)
[2019, 56(1):101-109]

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Giant right atrium and subvalvular pulmonary stenosis: A case report of an interesting combination.

Viviana Maestrini, Lucia I Birtolo, Sara Cimino, Paolo Severino, Massimo Mancone, Marco Francone, Sanjay M Banypersad, Flavia Ventriglia, Luigi Tritapepe, Fabio Miraldi, Francesco Fedele,

A 20-year-old Congolese woman presented with presyncope, dyspnea, and anasarca. Past medical history was unremarkable. Echocardiography revealed a rare combination of giant right atrium (RA), a dilated and hypertrophied right ventricle, subvalvular pulmonary stenosis (subPS), severe tricuspid regurgitation (TR), pericardial effusion and what appeared to be a spontaneously closed ventricular ... Read more >>

Echocardiography (Echocardiography (Mount Kisco, N.Y.))
[2019, 36(5):992-995]

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Pregnancy in Women with Complex Congenital Heart Disease. A Constant Challenge.

Walkiria Samuel Avila, Veronica Martins Ribeiro, Eduardo Giusti Rossi, Maria Angelica Binotto, Maria Rita Bortolotto, Carolina Testa, Rossana Francisco, Ludhmilla Abraão Hajjar, Nana Miura,

BACKGROUND:The improvement in surgical techniques has contributed to an increasing number of childbearing women with complex congenital heart disease (CCC). However, adequate counseling about pregnancy in this situation is uncertain, due to a wide variety of residual cardiac lesions. OBJECTIVES:To evaluate fetal and maternal outcomes in pregnant women with CCC ... Read more >>

Arq. Bras. Cardiol. (Arquivos brasileiros de cardiologia)
[2019, 113(6):1062-1069]

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Imaging of the aortic root on high-pitch non-gated and ECG-gated CT: awareness is the key!

Prashant Nagpal, Mukta D Agrawal, Sachin S Saboo, Sandeep Hedgire, Sarv Priya, Michael L Steigner,

The aortic pathologies are well recognized on imaging. However, conventionally cardiac and proximal aortic abnormalities were only seen on dedicated cardiac or aortic studies due to need for ECG gating. Advances in CT technology have allowed motionless imaging of the chest and abdomen, leading to an increased visualization of cardiac ... Read more >>

Insights Imaging (Insights into imaging)
[2020, 11(1):51]

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The science and art of aortic and/or pulmonary root translocation.

Supreet P Marathe, Sachin Talwar,

This review aims to present and compare different surgical techniques of root translocation of the great arteries except the Ross procedure. The historical aspects, technical considerations, and results are briefly elucidated. ... Read more >>

Ann Pediatr Cardiol (Annals of pediatric cardiology)
[2020, 13(1):56-66]

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Mutations in NRXN1 and NRXN2 in a patient with early-onset epileptic encephalopathy and respiratory depression.

Anne M Rochtus, Sara Trowbridge, Richard D Goldstein, Beth Rosen Sheidley, Sanjay P Prabhu, Robin Haynes, Hannah C Kinney, Annapurna H Poduri,

Early infantile epileptic encephalopathy (EIEE) is a severe disorder associated with epilepsy, developmental delay and intellectual disability, and in some cases premature mortality. We report the case of a female infant with EIEE and strikingly suppressed respiratory dysfunction that led to death. Postmortem research evaluation revealed hypoplasia of the arcuate ... Read more >>

Cold Spring Harb Mol Case Stud (Cold Spring Harbor molecular case studies)
[2019, 5(1):]

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Trileaflet reconstruction of pulmonary valve for acute pulmonary valve insufficiency.

Doğan Kahraman,

Iatrogenic pulmonary valve insufficiency is a life-threatening complication and its treatment options pose another challenge. Easily accessible mechanical valves have high complication rates. Xenografts and homografts are expensive materials and are not readily accessible in case of emergency. Although monoand bileaflet reconstructions with autologous pericardium in the pediatric population has ... Read more >>

Turk Gogus Kalp Damar Cerrahisi Derg (Turk gogus kalp damar cerrahisi dergisi)
[2019, 27(2):219-223]

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Double-orifice mitral valve repair.

Teresa Gonzalez, Francisco Vera, Enrique Ruiz,

We present the case of a 6-year-old patient with double-orifice mitral valve and severe regurgitation, which was successfully repaired. We demonstrate that mitral valve repair may be attempted even in complex anatomy such as the double-orifice mitral valve, where it can offer excellent results. ... Read more >>

Cardiol Young (Cardiology in the young)
[2019, 29(2):214-215]

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Management of Congenital Heart Disease: State of the Art-Part II-Cyanotic Heart Defects.

P Syamasundar Rao,

In this review management of the most common cyanotic congenital heart defects (CHDs) was discussed; the management of acyanotic CHD was reviewed in Part I of this series. While the need for intervention in acyanotic CHD is by and large determined by the severity of the lesion, most cyanotic CHDs ... Read more >>

Children (Basel) (Children)
[2019, 6(4):]

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Severe thrombocytopenia in tetralogy of Fallot patients: A contraindication for corrective surgery?

Suraj Patil, Jay Relan, Milind Hote, Shyam Sunder Kothari,

A 3-year-old boy with tetralogy of Fallot and recurrent cyanotic spells was found to have severe thrombocytopenia with platelet counts in the range of 11-30,000/mm3. There was a hesitation to operate in view of the high bleeding risk due to profound thrombocytopenia. However, the total correction was done after excluding ... Read more >>

Ann Pediatr Cardiol (Annals of pediatric cardiology)
[2019, 12(3):305-307]

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Pattern of un-operated Grown Up Congenital Heart (GUCH) patients presenting to a Tertiary Care Cardiac Institute of Punjab.

Abdul Razzaq Mughal, Rubina Tousif, Asif Rashid Alamgir, Anjum Jalal,

Objectives:To identify the pattern of un-operated grown up congenital heart defects at our tertiary care cardiac institute. Methods:This is a prospective observational study. All un-operated GUCH patients who presented to Faisalabad Institute of Cardiology (FIC) from May 2017 to 30th July 2017 were enrolled. Diagnosis was established on Transthoracic Echocardiography ... Read more >>

Pak J Med Sci (Pakistan journal of medical sciences)
[2019, 35(4):1066-1071]

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EDUCATIONAL SERIES IN CONGENITAL HEART DISEASE: Tetralogy of Fallot: diagnosis to long-term follow-up.

R Bedair, X Iriart,

Tetralogy of Fallot (TOF) is the most common cyanotic congenital heart defect, affecting 3 in 10,000 live births. Surgical correction in early childhood is associated with good outcomes, but lifelong follow-up is necessary to identify the long-term sequelae that may occur. This article will cover the diagnosis of TOF in ... Read more >>

Echo Res Pract (Echo research and practice)
[2019, 6(1):R9-R23]

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EDUCATIONAL SERIES IN CONGENITAL HEART DISEASE: Echocardiographic assessment of transposition of the great arteries and congenitally corrected transposition of the great arteries

Meryl S Cohen, Luc L Mertens,

Echocardiographic assessment of patients with transposition of the great arteries and congenitally corrected transposition requires awareness of the morphology and commonly associated lesions. The pre-operative echocardiography should include a full segmental and sequential analysis. Post-operative assessment is not possible without awareness of the type of surgical procedure performed and consists ... Read more >>

Echo Res Pract (Echo research and practice)
[2019, 6(4):R107-R119]

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Early right ventricular function following trans-right atrial versus trans-right atrial, trans-right ventricular repair of Tetralogy of Fallot: Results of a prospective randomized study.

Sachin Talwar, Abhishek Anand, Bharat Siddarth, Sivasubramanian Ramakrishnan, Shiv Kumar Choudhary, Balram Airan,

Objective:We compared the pre- and post-operative right ventricular (RV) function by tricuspid annular plane systolic excursion (TAPSE) between trans-right atrial (t-RA) versus t-RA/RV (RA/RV) approach for the repair of Tetralogy of Fallot (TOF). Patients and Methods:Fifty consecutive patients, 1-15 years of age, undergoing intracardiac repair of TOF between September 2015 ... Read more >>

Ann Pediatr Cardiol (Annals of pediatric cardiology)
[2019, 12(1):3-9]

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Double-Outlet Left Ventricle: The Importance of Echocardiographic and Computed Tomographic Assessment.

Ezequiel Sagray, M Yasir Qureshi, Thomas A Foley, Donald J Hagler, Patrick W O'Leary, Frank Cetta,

CASE (Phila) (CASE (Philadelphia, Pa.))
[2019, 3(4):141-144]

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