Marfan Syndrome: Regarding Two Cases

Bibliographic Details
Title: Marfan Syndrome: Regarding Two Cases
Authors: Elsy Roxana Geroy Moya, María Quiñones Hernández, Anaelys Acosta Hernández
Source: Revista Finlay, Vol 10, Iss 1, Pp 62-72 (2020)
Publisher Information: Universidad de las Ciencias Médicas de Cienfuegos, 2020.
Publication Year: 2020
Collection: LCC:Internal medicine
LCC:Special situations and conditions
Subject Terms: palabras clave: síndrome de marfán, enfermedades genéticas congénitas, enfermedades raras, diagnóstico, informes de casos, Internal medicine, RC31-1245, Special situations and conditions, RC952-1245
More Details: Marfan syndrome is an autosomal dominant genetic disorder, with a prevalence of 1 every 5,000-10,000 newborns, so it is classified as an uncommon disease. It affects multiple organs and systems; its prognosis is marked by the cardiovascular involvement. Multidisciplinary follow-up of these patients allows the timely diagnosis of complications and improves their quality of life. Two cases with Marfan syndrome and other associated diseases are presented. A literature review was carried out regarding the report of 2 teenager clinical cases with suggestive phenotypic characteristics, the first case with an associated arachnoidocele and the second case with Gilbert's disease.
Document Type: article
File Description: electronic resource
Language: Spanish; Castilian
ISSN: 2221-2434
Relation: http://www.revfinlay.sld.cu/index.php/finlay/article/view/793; https://doaj.org/toc/2221-2434
Access URL: https://doaj.org/article/96ba189b247547c59cbadd856191fa6b
Accession Number: edsdoj.96ba189b247547c59cbadd856191fa6b
Database: Directory of Open Access Journals
More Details
ISSN:22212434
Published in:Revista Finlay
Language:Spanish; Castilian