Systemic to Pulmonary Arterial Collaterals or Connections Associated with Pulmonary Vascular Disease

Cardiac phenotypic spectrum of KCNT1 mutations

Utkarsh Kohli, Chitra Ravishankar, Douglas NordliComer Children’s Hospital and Pritzker School of Medicine of the University of Chicago. he Children’s Hospital of Philadelphia and Perelman School of Medicine at the University of Pennsylvania. United States Cardiology in the YoungCardiol Young 2020; 30: 1935-1939DOI: 10.1017/S1047951120002735 AbstractWe report a 10-month-old girl with KCNT1 (c1420C > T; p. Arg474Cys, […]

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Isolated agenesis of the right pulmonary veins with pulmonary sequestration

Shilpa Patil, Sakshi Sachdeva, Shweta Bakhru, Bharat Dalvi, Nageswara Rao KonetiCare Hospital. Glenmark Cardiac Center. India Annals of Pediatric CardiologyAnn Pediatr Cardiol 2019; 12: 135-137DOI: 10.4103/apc.APC_55_18 AbstractWe report two cases of agenesis of the right pulmonary veins (PVs) associated with sequestration of the right lung with systemic to pulmonary collateral. Both the children were referred for

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Hypoplastic right lung associated with right pulmonary vein stenosis and systemic collateral

Anant Khositseth, Suvipaporn Siriporpitak, Preecha LaohakunakornRamathibodi Hospital Mahidol University.Thailand Congenital Heart DiseaseCongenit Heart Dis 2010; 5: 76-80DOI: 10.1111/j.1747-0803.2009.00324.x AbstractWe present a case of a 6-month-old girl diagnosed as unilateral pulmonary vein stenosis (right inferior pulmonary vein) with dextroposition of the heart, hypoplastic right lung, hypoplastic right pulmonary artery, collateral from the descending aorta supplied right lower

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Congenital isolated unilateral agenesis of pulmonary arteries in adults: case series and review

Pankaj Jariwala, Venkata Nagarjuna Maturu, Johann Christopher, Kartik Pandurang JadhavYashoda Hospitals. Care Hospitals.India Indian Journal of Thoracic and Cardiovascular SurgeryIndian J Thorac Cardiovasc Surg 2021; 37 (Suppl 1): 144-154DOI: 10.1007/s12055-020-01032-w AbstractCongenital, isolated unilateral agenesis of pulmonary arteries (UAPA) has a bimodal clinical presentation. It is either diagnosed in early infancy or during adulthood. Early diagnosis and

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Systemic artery to pulmonary artery aneurysm malformations associated with variants at MCF2L

S.E. Mitchell, R. P. Martin, P. Terry, S. E. Drant, D. Valle, H. Dietz, N. SobreiraJohns Hopkins University School of Medicine. Children’s Hospital of Philadelphia. United States American Journal of Medical GeneticsAm J Med Genet 2023; 191: 1250-1260DOI: 10.1002/ajmg.a.63141 AbstractArteriovenous malformations (AVM) are characterized by abnormal vessels connecting arteries and veins resulting in a disruption of

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Multifactorial pulmonary hypertension in infantile scimitar syndrome

Damien Bonnet, Isabelle Szezepanski, Christophe Delacourt, Sophie Malkezadeh-Milani, Maryline LévyHôpital Necker-Enfants Malades, AP-HP, Université de ParisFrance Archives of Cardiovascular DiseaseArch Cardiovasc Dis 2022; 115: 142-150DOI: 10.1016/j.acvd.2022.01.004 AbstractBackground: Pulmonary hypertension in infantile scimitar syndrome is highly prevalent at diagnosis, and has a multifactorial origin.Aims: To analyse the constellation of anatomical anomalies and initial physiology, and their contribution to

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