Cardiovocal syndrome or Ortner’s can be caused due to a myriad of etiologies in the neck mediastinum. The also consequence many cardiac mediastinal pathologies even complications surgical treatment. objective this research was systematically review provide an overview etiopathogenesis syndrome. Cochrane Handbook for Systematic Reviews used methodology and adhered “Preferred Reporting Items Revi...

BACKGROUND AND PURPOSE Marfan syndrome is a heritable disorder of connective tissue caused by a deficiency of the glycoprotein fibrillin. In several publications and neurological textbooks, a relationship between Marfan syndrome and intracranial aneurysms has been assumed. METHODS The records of 135 patients classified as having Marfan syndrome who visited the Amsterdam Marfan clinic or were ...

DESCRIPTION Coronary slow flow (CSF) is a phenomenon characterised by delayed opacification of coronary arteries in the absence of epicardial stenosis, in which microvascular and endothelial dysfunction have been implicated in pathophysiology. The association between acute coronary syndromes (ACS) and Behcet’s syndrome is well known but rare, and is especially important due to the tendency to a...

It is well known that about one-third of the patients with Turner's syndrome have coarctation of the aorta; however, only a relatively small number of patients with Turner's syndrome and coarctation of the aorta have been found to also have an aortic aneurysm Patients with Turner's syndrome and aortic aneurysm but without coarctation of the aorta have been documented even less frequently.'" We ...

Abbreviations: ACS: Abdominal Compartment Syndrome; APACHE-II: Acute Physiology and Chronic Health Evaluation II; CT: Computed Tomography; CVVH: Continuous Renal Replacement Therapy; DCO: Damage Control Operation; EVAR: Endovascular Aneurysm Repair; IAH: Intra-abdominal Hypertension; IAP: Intraabdominal Pressure; ICU: Intensive Care Unit; MODS: Multiple Organ Dysfunction Syndrome; rAAA: Rupture...

OBJECTIVE To determine the symptoms experienced by patients diagnosed with Behcet's Disease and how they cope with them. METHODS The qualitative study was conducted from September 2013 to March 2014 at Ege University Medical Faculty Hospital, Turkey, comprising patients having all symptoms of Behcet's Disease. Data was collected through semi-structured focus-group interview form. The findings...

Behcet disease (BD) is a chronic, multisystem, inflammatory disease characterized by variable clinical manifestations involving systemic vasculitis of both the small and large blood vessels. The majority of BD patients present with recurrent oral ulcers in combination with other manifestations of the disease, including genital ulcers, skin lesions, arthritis, uveitis, thrombophlebitis, gastroin...

We report new findings from a neurological case described by Hanley, Young, and Pearson (1989). In the original study, the patient, BD, had impaired biographical knowledge of people which appeared to extend to a general impairment of knowledge of “living things”. In more recent work, we present evidence which confirms Hanley et al.’s finding that BD has impaired person-specific knowledge, but w...