Journal of Rare Cardiovascular Diseases: Your guide to the latest developments in the field – and to your RCD patient management
Journal Title: Journal of Rare Cardiovascular Diseases - Year 2013, Vol 1, Issue 4
Abstract
Dear Readers, Dear Friends and Colleagues, It is a pleasure to deliver at your hand the next (already the fourth!) issue of your quarterly Journal of Rare Cardiovascular Diseases. We are happy that, with your continued submissions, we are able to publish the journal regularly, and that the Journal has established its natural presence in the family of cardiovascular journals. Fulfilling the principal aim of the Journal, the submissions to this issue have been accepted on a key basis of their relevance to your expanding knowledge and management of your Rare Cardiovascular Disease (RCD) patients. We begin with a review on Ebstein anomaly by a prominent paediatric cardiac surgeon, Dr Jacek Pajak, who performed complex surgeries in a some key centers in the world prior to taking the position of the Head of Paeditric Cardiac Sugery in the Medical University of Silesia in Katowice. Ebstein anomaly patients pose significant decision‑making challenges in every‑day clinical practice of RCD.
Authors and Affiliations
Piotr Podolec
Rare diseases: a priority in public health and research
Since the 1990s at both European Union (EU) and country level political concepts and initiatives concerning rare diseases have emerged. At European level, there are currently three key policy documents establishing a pol...
Broad QRS complex tachycardia in a patient with myotonic dystrophy (Steinert disease) (RCD code: V‑4O)
Myotonic dystrophy is a rare inherited condition affecting primarily skeletal muscles and commonly associated with cardiovascular pathology. We report a case of a 50- year old female with myotonic dystrophy type 1 who pr...
“One of the greatest disease is to be nobody to anybody”
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A 33-year-old man after sudden cardiac arrest as a first manifestation of Brugada syndrome (RCD code: V‑1A.1)
Brugada syndrome is an autosomal dominant genetic disease with variable expression characterized by abnormal electrocardiographic findings – right bundle branch block and ST-segment elevation in the anterior precordial l...
Right atrial myxoma in a patient with Budd‐Chiari syndrome
Budd‐Chiari syndrome (BCS) is a rare clinical disorder which is caused by obstruction of the major hepatic veins or suprahepatic portion of the inferior vena cava. Either thrombosis or a mechanical venous obstruction may...