MANAGEMENT OF YOUNG PATIENTS WITH MARFAN SYNDROME
نویسندگان
چکیده
منابع مشابه
Management of Marfan syndrome.
Marfan syndrome is a variable, autosomal dominant connective tissue disorder, affecting mainly the cardiovascular system, eyes, and skeleton. The incidence is approximately 1 in 9800, and around 26% of cases have no family history, the condition resulting from a new mutation. Characteristic features include progressive aortic dilatation associated with aortic valve incompetence, mitral valve pr...
متن کاملThe Characteristics of Acute Aortic Dissection among Young Chinese Patients: A Comparison between Marfan Syndrome and Non-Marfan Syndrome Patients
PURPOSE Aortic dissection (AoD) is one of the most common catastrophes involving the aorta. Nevertheless, early diagnosis remains to be a challenge in the Emergency Department (ED), particularly in young individuals. In this study, we attempted to identify the characteristics of acute AoD among young individuals, particular in patients with Marfan syndrome. MATERIALS AND METHODS This was an r...
متن کاملMedical management of Marfan syndrome.
Marfan syndrome is an autosomal dominant, multisystem disease characterized by long bone overgrowth and other skeletal abnormalities, dislocation of the ocular lens, pneumothorax, decreased skeletal muscle mass, mitral valve prolapse, and dilatation of the aortic root. Antoine BernardJean Marfan first described the syndrome in 1896 in a young patient with peculiarly long and thin digits (subseq...
متن کاملPulmonary disease in patients with Marfan syndrome.
Hospital case notes and chest radiographs of 100 patients with Marfan syndrome were investigated for evidence of pulmonary disease. The criteria for inclusion of details of a given patient in the study were the occurrence of Marfan abnormalities in at least two separate body systems (skeletal, cardiovascular, ocular) or in one body system where there was a family history of a classically affect...
متن کاملUnprovoked Pulmonary Embolism in a Young Patient with Marfan Syndrome
Marfan syndrome is a rare connective tissue disorder with a prevalence of approximately 2 to 3 per 10,000 individuals. There have been some reports of young patients with Marfan syndrome developing arteriovenous thromboembolism. These events were unprovoked and recurrent. Owing to its rarity, hypercoagulopathy and other metabolic derangement in patients with Marfan syndrome remains largely unkn...
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ژورنال
عنوان ژورنال: Russian Pediatric Journal
سال: 2019
ISSN: 2413-2918,1560-9561
DOI: 10.18821/1560-9561-2019-22-6-395-400