Grönblad-Strandberg syndrome. Presentation of a patient

Syndrome Grönblad-Strandberg is a rare hereditary disease it is a genetic disorder of connective tissue characterized by fragmentation of elastic fibers and subsequent calcification affecting the dermis, blood vessels and Bruch's membrane of retina. The inheritance pattern is highly variable, m...

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Bibliographic Details
Main Authors: Zoila Fariñas Falcón, Rubén Antoliano Rangel Fleites, Amarilis Hernández Camacho
Format: Article
Language:Spanish
Published: Editorial Ciencias Médicas 2014-06-01
Series:Acta Médica del Centro
Subjects:
Online Access:http://www.revactamedicacentro.sld.cu/index.php/amc/article/view/134