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[Vascular Ehlers-Danlos syndrome].
- Source :
-
Presse medicale (Paris, France : 1983) [Presse Med] 2006 Dec; Vol. 35 (12 Pt 2), pp. 1864-75. - Publication Year :
- 2006
-
Abstract
- The vascular type of Ehlers-Danlos syndrome (EDS) is a rare genetic disease transmitted as an autosomal dominant trait. It is distinguished from other forms of EDS by its unstable acrogeric morphotype and by vascular, gastrointestinal, and obstetrical complications. Diagnosis is based on various clinical signs, noninvasive imaging, and on the identification of a mutation of the COL3A1 gene, which provides diagnostic certainty but has a sensitivity of only 61%. When two major diagnostic criteria are present, a genetic test should be proposed, performed and its result presented in a multidisciplinary group. The precautionary principle requires that preventive measures be implemented when the diagnosis is suspected. All artery puncture, surgery, and gastrointestinal and uterine endoscopy are contraindicated, permissible only in life-threatening emergencies. Straining against a closed glottis and all other situations or drugs likely to raise blood pressure must be avoided. Contraception must be discussed to avoid pregnancy during the diagnostic period. Arterial lesions suggestive of the disease include dissecting aneurysms of the internal carotid and iliac arteries and of the anterior visceral branches of the abdominal aorta, fusiform aneurysms of the splenic artery, and early onset nontraumatic direct carotid-cavernous fistulae. Early-onset varicose veins, spontaneous peritonitis or unusually important perineal lesions after giving birth should also attract the physician's attention. Psychological treatment and support of patients and their families is essential, to help them both to live with their disease and to deal with the information and screening issues. The prognosis of Ehlers-Danlos syndrome, vascular type, is grim but there is wide interindividual variability and life expectancy is best among patients receiving regular follow-up. Management by an experienced multidisciplinary team, implementation of drastic prevention measures and, depending on the results of the BBEST study, the possible prescription of beta-blockers should help to reduce the risk of complications and justify hope for a real improvement in prognosis in the near future.
- Subjects :
- Adult
Ascorbic Acid therapeutic use
Celiprolol therapeutic use
Child
Clinical Trials as Topic
Collagen Type III genetics
Contraception
Female
Genetic Counseling
Humans
Male
Mutation
Phenotype
Pregnancy
Pregnancy Complications
Prognosis
Tomography, X-Ray Computed
Ultrasonography, Doppler
Vasodilator Agents therapeutic use
Ehlers-Danlos Syndrome complications
Ehlers-Danlos Syndrome diagnosis
Ehlers-Danlos Syndrome diagnostic imaging
Ehlers-Danlos Syndrome drug therapy
Ehlers-Danlos Syndrome genetics
Ehlers-Danlos Syndrome physiopathology
Ehlers-Danlos Syndrome therapy
Subjects
Details
- Language :
- French
- ISSN :
- 0755-4982
- Volume :
- 35
- Issue :
- 12 Pt 2
- Database :
- MEDLINE
- Journal :
- Presse medicale (Paris, France : 1983)
- Publication Type :
- Academic Journal
- Accession number :
- 17159712
- Full Text :
- https://doi.org/10.1016/s0755-4982(06)74919-3