SciELO - Scientific Electronic Library Online

 
vol.115 issue4Multinucleated normoblastemia in a newborn secondary to hypoxiaTwo novel mutations in the glycine decarboxylase gene in a boy with classic nonketotic hyperglycinemia: case report author indexsubject indexarticles search
Home Pagealphabetic serial listing  

Services on Demand

Journal

Article

Indicators

  • Have no cited articlesCited by SciELO

Related links

  • Have no similar articlesSimilars in SciELO

Share


Archivos argentinos de pediatría

Print version ISSN 0325-0075On-line version ISSN 1668-3501

Abstract

ROSENTAL, Carlos F et al. Loeys-Dietz Syndrome, 3 generations, 4 familial cases. Arch. argent. pediatr. [online]. 2017, vol.115, n.4, pp.e220-e224. ISSN 0325-0075.  http://dx.doi.org/10.5546/aap.2017.e220.

Loeys-Dietz Syndrome is an autosomal dominant disease with aortic aneurysms, arterial tortuosity with hypertelorism and bifid uvula. We describe four familial cases within three generations. The diagnosis, surgical management and followup will be addressed.

Keywords : Loeys-Dietz syndrome; Aortic aneurysm; Aortic dissection.

        · abstract in Spanish     · text in Spanish     · Spanish ( pdf )

 

Creative Commons License All the contents of this journal, except where otherwise noted, is licensed under a Creative Commons Attribution License