Go to:
Logótipo
Comuta visibilidade da coluna esquerda
Você está em: Start > Publications > View > Vascular Ehlers-Danlos syndrome: a case with fatal outcome.
Publication

Publications

Vascular Ehlers-Danlos syndrome: a case with fatal outcome.

Title
Vascular Ehlers-Danlos syndrome: a case with fatal outcome.
Type
Article in International Scientific Journal
Year
2011
Authors
Morais, P
(Author)
Other
The person does not belong to the institution. The person does not belong to the institution. The person does not belong to the institution. Without AUTHENTICUS Without ORCID
Alberto Mota
(Author)
FMUP
View Personal Page You do not have permissions to view the institutional email. Search for Participant Publications View Authenticus page View ORCID page
Eloy, C
(Author)
Other
The person does not belong to the institution. The person does not belong to the institution. The person does not belong to the institution. Without AUTHENTICUS Without ORCID
Lopes, JM
(Author)
FMUP
View Personal Page You do not have permissions to view the institutional email. Search for Participant Publications View Authenticus page View ORCID page
Torres, F
(Author)
Other
The person does not belong to the institution. The person does not belong to the institution. The person does not belong to the institution. Without AUTHENTICUS Without ORCID
Palmeiro, A
(Author)
Other
The person does not belong to the institution. The person does not belong to the institution. The person does not belong to the institution. Without AUTHENTICUS Without ORCID
Tavares, P
(Author)
Other
The person does not belong to the institution. The person does not belong to the institution. The person does not belong to the institution. Without AUTHENTICUS Without ORCID
Azevedo, F
(Author)
Other
The person does not belong to the institution. The person does not belong to the institution. The person does not belong to the institution. Without AUTHENTICUS Without ORCID
Journal
Vol. 17
Final page: 1
ISSN: 1087-2108
Indexing
Other information
Authenticus ID: P-007-ZCY
Abstract (EN): A 13-year-old boy, born prematurely and hypotonic, from non-consanguineous healthy parents, was referred to our department because of easy bruising. A slightly extensible, thin and translucent skin, associated with dysmorphic facies, acrogeria, multiple ecchymoses, hypermobility of the small joints, dorsal kyphosis, genu valgum, flat feet, elongated upper limbs, and low muscle tone were all evident. A history of learning disability and bilateral inguinal hernia was present. Blood and imaging studies were unremarkable. A skin biopsy disclosed an unremarkable dermis; electron microscopy showed abnormalities in the diameter, contour, and shape of collagen fibrils/fibers. Genetic analysis revealed heterozygosity for a novel mutation in COL3A1 gene (c.3527G>A), confirming the diagnosis of vascular Ehlers-Danlos syndrome (VEDS). The patient died at 15 years of age because of aortic dissection. Vascular Ehlers-Danlos syndrome is a rare, life-threatening, autosomal dominant variant of EDS, resulting from mutations in COL3A1 gene. Affected individuals are prone to serious and potentially fatal complications, especially vascular, intestinal, and uterine ruptures. Delay in diagnosis is common, even when the clinical presentation is typical. Therefore, dermatologists should be familiar with VEDS features because the skin findings may be the first signs. Early diagnosis will improve management of visceral complications and allow early genetic counseling.
Language: English
Type (Professor's evaluation): Scientific
Documents
We could not find any documents associated to the publication.
Related Publications

Of the same journal

Unknown: Bilateral symmetrical papules on the eyelid (2009)
Another Publication in an International Scientific Journal
Duarte, AF; Nogueira, A; Carmen Silva; Azevedo, F
The spectrum of focal epithelial hyperplasia-a report of two cases (2021)
Another Publication in an International Scientific Journal
Cerejeira, A; Gomes, N; Melo, D; Sobrinho-Simões, J; Azevedo, F; Carmen Silva
Letter: Incontinentia pigmenti with vesicular stage in utero (2010)
Another Publication in an International Scientific Journal
Osorio, F; magina, s; Nogueira, A; Azevedo, F
Dermatitis artefacta (2021)
Another Publication in an International Scientific Journal
Cerejeira, A; Gomes, N; Cruz, M; Alberto Mota; Azevedo, F
Cutaneous Richter syndrome mimicking a lower limb cellulitis infection - A case report and review of the literature (2016)
Another Publication in an International Scientific Journal
César, A; Calistru, A; Pardal, J; magina, s; Alberto Mota; Azevedo, F

See all (32)

Recommend this page Top
Copyright 1996-2025 © Faculdade de Direito da Universidade do Porto  I Terms and Conditions  I Acessibility  I Index A-Z
Page created on: 2025-08-25 at 11:41:58 | Privacy Policy | Personal Data Protection Policy | Whistleblowing