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About 441 results

ALLMedicine™ Vascular Ehlers-Danlos Syndrome Center

Research & Reviews  219 results

Intraperitoneal bladder rupture in a young child with vascular Ehlers-Danlos syndrome.
https://doi.org/10.1002/ajmg.a.62004
American Journal of Medical Genetics. Part A; Nanduri R, Jones E et. al.

Feb 15th, 2021 - In this report, we present the case of a 3-year-old child with vascular Ehlers-Danlos syndrome (vEDS) previously known as Ehlers-Danlos syndrome type IV. After experiencing a minor traumatic injury to the abdomen, consisting of falling over a bath...

Role of Clinical Genetic Testing in the Management of Aortopathies.
https://doi.org/10.1007/s11886-020-01435-6 10.1016/j.amjcard.2007.10.039 10.1097/01.gim.0000195973.60136.48 10.1097/MOP.0000000000000836 10.1038/sj.ejhg.5200582 10.1161/CIRCGEN.117.002058 10.1136/heartjnl-2016-310631 10.1093/eurheartj/ehv739 10.1136/jmedgenet-2018-105583 10.1038/gim.2014.72 10.1161/CIRCGENETICS.114.000943 10.1038/s41436-018-0038-0 10.1038/s41436-018-0399-4 10.1136/jmg.2009.072785 10.1038/gim.2014.11 10.1002/ajmg.c.31553 10.1016/j.athoracsur.2006.04.098 10.1016/S0741-5214(97)70261-1 10.1161/circulationaha.120.045990 10.1038/s41436-019-0444-y 10.1038/s41436-019-0435-z 10.1016/j.jacc.2017.09.1094 10.1038/nrcardio.2016.211 10.1038/s41436-018-0356-2 10.1016/j.jvs.2017.12.023 10.1016/j.jacc.2018.04.089 10.1056/NEJMsr1406261 10.1038/gim.2015.30 10.1161/CIRCGEN.117.002039 10.1038/s41576-018-0018-x 10.1161/CIR.0b013e3181d4739e 10.1007/s10897-014-9743-2 10.1161/HCG.0000000000000054 10.1016/j.hrthm.2011.07.017 10.1056/NEJM199405123301902 10.1126/science.1124287 10.1016/j.ahj.2007.06.024 10.1056/NEJMoa1404731 10.1016/S0140-6736(19)32518-8 10.1161/CIRCGENETICS.116.001485 10.1038/ng1511 10.1161/CIRCULATIONAHA.110.990549 10.1038/gim.2014.53 10.1161/JAHA.116.004052 10.1016/j.amjcard.2016.09.024 10.1016/j.jacc.2012.03.051
Current Cardiology Reports; Harris SL, Lindsay ME

Jan 21st, 2021 - Thoracic aortic aneurysms (TAA) have a strong heritable basis, and identification of a genetic etiology has important implications for patients with TAA and their relatives. This review provides an overview of Mendelian causes of TAA, discusses im...

Cardiogenetics: genetic testing in the diagnosis and management of patients with aortic...
https://doi.org/10.1136/heartjnl-2020-317036
Heart (British Cardiac Society); Thakker PD, Braverman AC

Dec 18th, 2020 - Thoracic aortic aneurysm and aortic dissection have a potent genetic underpinning with 20% of individuals having an affected relative. Heritable thoracic aortic diseases (HTAD) may be classified as syndromic (including Marfan syndrome, Loeys-Dietz...

Celiprolol Treatment in Patients with Vascular Ehlers-Danlos Syndrome.
https://doi.org/10.1016/j.ejvs.2020.10.020
European Journal of Vascular and endoVascular Surgery : T... Baderkhan H, Wanhainen A et. al.

Nov 23rd, 2020 - Vascular Ehlers-Danlos syndrome (vEDS) is a rare monogenetic disease caused by pathogenic variants in procollagen 3A1. Arterial rupture is the most serious clinical manifestation. A randomised controlled trial, the Beta-Blockers in Ehlers-Danlos S...

Medical Therapy Affects the Arteriopathy of Vascular Ehlers-Danlos Syndrome.
https://doi.org/10.1016/j.ejvs.2020.10.005
European Journal of Vascular and endoVascular Surgery : T... Kelly J, Lyons O

Nov 23rd, 2020 - Medical Therapy Affects the Arteriopathy of Vascular Ehlers-Danlos Syndrome.|2020|Kelly J,Lyons O,|

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Clinicaltrials.gov  221 results

Intraperitoneal bladder rupture in a young child with vascular Ehlers-Danlos syndrome.
https://doi.org/10.1002/ajmg.a.62004
American Journal of Medical Genetics. Part A; Nanduri R, Jones E et. al.

Feb 15th, 2021 - In this report, we present the case of a 3-year-old child with vascular Ehlers-Danlos syndrome (vEDS) previously known as Ehlers-Danlos syndrome type IV. After experiencing a minor traumatic injury to the abdomen, consisting of falling over a bath...

Role of Clinical Genetic Testing in the Management of Aortopathies.
https://doi.org/10.1007/s11886-020-01435-6 10.1016/j.amjcard.2007.10.039 10.1097/01.gim.0000195973.60136.48 10.1097/MOP.0000000000000836 10.1038/sj.ejhg.5200582 10.1161/CIRCGEN.117.002058 10.1136/heartjnl-2016-310631 10.1093/eurheartj/ehv739 10.1136/jmedgenet-2018-105583 10.1038/gim.2014.72 10.1161/CIRCGENETICS.114.000943 10.1038/s41436-018-0038-0 10.1038/s41436-018-0399-4 10.1136/jmg.2009.072785 10.1038/gim.2014.11 10.1002/ajmg.c.31553 10.1016/j.athoracsur.2006.04.098 10.1016/S0741-5214(97)70261-1 10.1161/circulationaha.120.045990 10.1038/s41436-019-0444-y 10.1038/s41436-019-0435-z 10.1016/j.jacc.2017.09.1094 10.1038/nrcardio.2016.211 10.1038/s41436-018-0356-2 10.1016/j.jvs.2017.12.023 10.1016/j.jacc.2018.04.089 10.1056/NEJMsr1406261 10.1038/gim.2015.30 10.1161/CIRCGEN.117.002039 10.1038/s41576-018-0018-x 10.1161/CIR.0b013e3181d4739e 10.1007/s10897-014-9743-2 10.1161/HCG.0000000000000054 10.1016/j.hrthm.2011.07.017 10.1056/NEJM199405123301902 10.1126/science.1124287 10.1016/j.ahj.2007.06.024 10.1056/NEJMoa1404731 10.1016/S0140-6736(19)32518-8 10.1161/CIRCGENETICS.116.001485 10.1038/ng1511 10.1161/CIRCULATIONAHA.110.990549 10.1038/gim.2014.53 10.1161/JAHA.116.004052 10.1016/j.amjcard.2016.09.024 10.1016/j.jacc.2012.03.051
Current Cardiology Reports; Harris SL, Lindsay ME

Jan 21st, 2021 - Thoracic aortic aneurysms (TAA) have a strong heritable basis, and identification of a genetic etiology has important implications for patients with TAA and their relatives. This review provides an overview of Mendelian causes of TAA, discusses im...

Cardiogenetics: genetic testing in the diagnosis and management of patients with aortic...
https://doi.org/10.1136/heartjnl-2020-317036
Heart (British Cardiac Society); Thakker PD, Braverman AC

Dec 18th, 2020 - Thoracic aortic aneurysm and aortic dissection have a potent genetic underpinning with 20% of individuals having an affected relative. Heritable thoracic aortic diseases (HTAD) may be classified as syndromic (including Marfan syndrome, Loeys-Dietz...

Celiprolol Treatment in Patients with Vascular Ehlers-Danlos Syndrome.
https://doi.org/10.1016/j.ejvs.2020.10.020
European Journal of Vascular and endoVascular Surgery : T... Baderkhan H, Wanhainen A et. al.

Nov 23rd, 2020 - Vascular Ehlers-Danlos syndrome (vEDS) is a rare monogenetic disease caused by pathogenic variants in procollagen 3A1. Arterial rupture is the most serious clinical manifestation. A randomised controlled trial, the Beta-Blockers in Ehlers-Danlos S...

Medical Therapy Affects the Arteriopathy of Vascular Ehlers-Danlos Syndrome.
https://doi.org/10.1016/j.ejvs.2020.10.005
European Journal of Vascular and endoVascular Surgery : T... Kelly J, Lyons O

Nov 23rd, 2020 - Medical Therapy Affects the Arteriopathy of Vascular Ehlers-Danlos Syndrome.|2020|Kelly J,Lyons O,|

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News  1 results

FDA declines to approve Acer Therapeutics' rare genetic disorder treatment
https://www.reuters.com/article/us-acer-therape-fda/fda-declines-to-approve-acer-therapeutics-rare-genetic-disorder-treatment-idUSKCN1TQ1K9

Jun 25th, 2019 - (Reuters) - Acer Therapeutics Inc said on Tuesday the U.S. Food and Drug Administration declined to approve its treatment for a severe, rare genetic disorder that can cause blood vessels to fatally rupture, sending its shares plunging as much as 7...

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