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A Forme Fruste of Marfan Syndrome: A Case Report

Marfan syndrome (MFS), an inherited connective tissue disorder, is caused by a mutation in the FBN1 gene. MFS is characterized by manifestations in the musculoskeletal system (joint laxity, scoliosis), the cardiovascular system (aortic dilation), and the ocular system (ectopic lens). We report a cas...

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Detalles Bibliográficos
Autores principales: Alsheikh, Nejood, Hawsawi, Samira A, AlGhamdi, Abeer, Alkhwaiter, Lolo, Alsulimani, Aseel, Suliman, Ihab
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9730431/
https://www.ncbi.nlm.nih.gov/pubmed/36505128
http://dx.doi.org/10.7759/cureus.31231