Congenital plaque-type glomuvenous malformation associated with chylous ascites

dc.contributor.author	Tejedor, Maria
dc.contributor.author	Martín-Santiago, Ana
dc.contributor.author	Gómez, Cristina
dc.contributor.author	Fiol, Miquel
dc.contributor.author	Benítez-Segura, Ignacio
dc.date.accessioned	2020-01-23T08:53:42Z
dc.identifier.uri	http://hdl.handle.net/11201/150682
dc.description.abstract	[eng] Glomuvenous malformations are hereditary vascular anomalies, usually without extracutaneous involvement. We report two cases of extensive thoracic plaque‐type glomuvenous malformation in newborns who had previously been diagnosed in utero with pleural effusion and ascites, suggesting a pathogenic link between the two conditions.
dc.format	application/pdf
dc.relation.isformatof	https://doi.org/10.1111/j.1525-1470.2010.01216.x
dc.relation.ispartof	Pediatric Dermatology, 2010, vol. 28, num. 5, p. 528-531
dc.rights	, 2010
dc.subject.classification	61 - Medicina
dc.subject.other	61 - Medical sciences
dc.title	Congenital plaque-type glomuvenous malformation associated with chylous ascites
dc.type	info:eu-repo/semantics/article
dc.date.updated	2020-01-23T08:53:42Z
dc.date.embargoEndDate	info:eu-repo/date/embargoEnd/2026-12-31
dc.embargo	2026-12-31
dc.rights.accessRights	info:eu-repo/semantics/embargoedAccess
dc.identifier.doi	https://doi.org/10.1111/j.1525-1470.2010.01216.x