Cargando…
Ehlers-Danlos syndrome type IV
Ehlers-Danlos syndrome type IV, the vascular type of Ehlers-Danlos syndromes (EDS), is an inherited connective tissue disorder defined by characteristic facial features (acrogeria) in most patients, translucent skin with highly visible subcutaneous vessels on the trunk and lower back, easy bruising,...
Autor principal: | Germain, Dominique P |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2007
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1971255/ https://www.ncbi.nlm.nih.gov/pubmed/17640391 http://dx.doi.org/10.1186/1750-1172-2-32 |
Ejemplares similares
-
Spontaneous Carotid-Cavernous Fistula in the Type IV Ehlers-Danlos Syndrome
por: Kim, Jeong Gyun, et al.
Publicado: (2014) -
Endovascular Management of Vascular Complications in Ehlers–Danlos Syndrome Type IV
por: Alqahtani, Mubarak, et al.
Publicado: (2022) -
Ehlers-Danlos syndrome
por: Taj, Farhana Tahseen, et al.
Publicado: (2014) -
Perisigmoid Abscess Leading to a Diagnosis of Ehlers-Danlos Syndrome Type IV
por: Normatov, Inessa, et al.
Publicado: (2016) -
Ehlers–Danlos syndrome type IV as the etiology of spontaneous coronary artery rupture
por: Nishigaki, Kazuhiko
Publicado: (2012)