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 |