Marfan syndrome. Report of a patient
Marfan syndrome is a congenital hereditary disease (sporadic in 15-30% of cases) of connective tissue, dominant autosomal with complete penetrance, with prevalence estimated at one per 5 000 people and incidence of one per 10 000 births without racial or sex predominance. A patient with sporadic Mar...
Main Authors: | Luis Alberto Santos Pérez, Eric González Fernández, Cándida Grisel Milián Hernández |
---|---|
Format: | Article |
Language: | Spanish |
Published: |
Editorial Ciencias Médicas
2015-12-01
|
Series: | Acta Médica del Centro |
Subjects: | |
Online Access: | http://www.revactamedicacentro.sld.cu/index.php/amc/article/view/292 |
Similar Items
-
Marfan Syndrome: Regarding Two Cases
by: Elsy Roxana Geroy Moya, et al.
Published: (2020-02-01) -
Marfan Syndrome: Regarding Two Cases
by: Elsy Roxana Geroy Moya, et al.
Published: (2020-02-01) -
Síndrome de Marfan. Presentación de un caso
by: Laydamí Rodríguez Amador, et al.
Published: (2022-07-01) -
Marfan Syndrome. Presentation of a case
by: Evelyn Johana Peñafiel-Criollo, et al.
Published: (2022-12-01) -
Costello Syndrome. A case report
by: Yadelis Maldonado Martínez, et al.
Published: (2014-06-01)