Cargando…
A Case of Near Total Aortic Replacement in an Adolescent With Loeys-Dietz Syndrome
Loeys-Dietz syndrome is a recently described autosomal dominant disorder caused by mutations in the genes for transforming growth factor-beta receptor type 1 or 2 (TGF-ßR 1/2). The syndrome predisposes patients to aortic aneurysm and dissections, along with craniofacial and musculoskeletal abnormali...
Autores principales: | Suh, Yoon Jung, Kwon, Hye Won, Kim, Gi Beom, Kwon, Bo Sang, Bae, Eun Jung, Noh, Chung Il, Choi, Jung Yun, Kim, Kyung Hwan, Kim, Yong Jin, Park, Sung Sup |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Korean Society of Cardiology
2012
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3341429/ https://www.ncbi.nlm.nih.gov/pubmed/22563345 http://dx.doi.org/10.4070/kcj.2012.42.4.288 |
Ejemplares similares
-
Valve Sparing Aortic Root Replacement in Children with Loeys-Dietz Syndrome
por: Sim, Hyung-Tae, et al.
Publicado: (2015) -
Multiple Aortic Operations in Loeys-Dietz Syndrome: Report of 2 Cases
por: Na, Kwon Joong, et al.
Publicado: (2014) -
Cleft Palate and Aortic Dilatation as Clues for Loeys–Dietz Syndrome
por: Zaza, Pierluigi, et al.
Publicado: (2022) -
The relation of aortic dimensions and obesity in adults with Marfan or Loeys-Dietz syndrome
por: Suleiman, Mathieu N., et al.
Publicado: (2022) -
Valve-sparing aortic root replacement in Loeys-Dietz syndrome and a novel mutation in TGFBR2
por: Kasar, Taner, et al.
Publicado: (2018)