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Author Archives: VASCERN Coordination

Recording of the VASCERN webinar: Classification of vascular anomalies now available!

The first live webinar from our Vascular Anomalies Working Group (VASCA-WG) was held on April 28th, 2021 and focused on the “Classification of vascular anomalies”. This webinar started with a brief presentation of the VASCA-WG by surprise guest, Prof. Miikka VIKKULA (Chair of the VASCA-WG), who equally announced the publication…

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May 4, 2021
EURORDIS recommendations to achieve a mature ERN system in 2030

In December 2020, EURORDIS and the European Patient Advocacy Group (ePAG) patient advocates published a paper, which reviews the progress achieved so far and presents their vision of a mature European Reference Network (ERN) system. “Our vision is for a mature ERN system that leaves no person living with a…

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December 17, 2020
5 new training videos on how to use CPMS now available!

Ibrahim Donmez, our IT Helpdesk & End User Support Specialist, has made 5 new training videos regarding the use of the Clinical Patient Management System (CPMS) and they are now available to view! These short videos aim to assist our users to master some of the key steps involved in enrolling…

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September 25, 2020
Six new language subtitles added to the Pills of Knowledge video on Klippel-Trenaunay syndrome!

The Pill of Knowledge (PoK) video on Klippel-Trenaunay syndrome (KTS) has just had 6 new language subtitles added! Since its publication in January 2020, VASCERN members of the Vascular Anomalies Working Group (VASCA-WG) have been working on translating the English subtitles and thanks to their help, the subtitles have been…

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September 7, 2020
A look back at the Pediatric and Primary Lymphedema Working Group’s 2-day Virtual Meeting!

The Pediatric and Primary Lymphedema Working Group (PPL WG) face-to-face meeting was scheduled in Helsinki but due to COVID-19, it had to be cancelled and was held online from June 4th to 5th, 2020. This virtual meeting was chaired by Dr. Robert Damstra and attended by 14 healthcare professionals from…

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June 17, 2020
Review of the Vascular Anomalies Working Group’s 2-day Virtual Meeting!

The Vascular Anomalies Working Group (VASCA WG) face-to-face meeting, that was planned to take place in Brussels from April 28th to 29th, 2020 was instead transformed into a 2-day virtual meeting due to COVID-19. Chaired by Professor Miikka Vikkula, the meeting was attended by 14 healthcare professionals from 10 EU…

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May 6, 2020
New Pill of Knowledge – Role of patient advocates in the ERNs from the HTAD ePAG

We have just released a new Pill of Knowledge (PoK) video on our YouTube channel entitled “Role of patient advocates in a European Reference Network, from the patient team of Heritable Thoracic Aortic Diseases (HTAD)“. This Pill of Knowledge features members of the HTAD European Patient Advocacy group (ePAG) explain…

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September 9, 2019
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    Familial forms of bicuspid aortic valve with aortopathy

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    Rare disease with thoracic aortic aneurysm and aortic dissection

    Medium Sized Arteries

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    Pediatric and Primary Lymphedema

    Anhidrotic ectodermal dysplasia-immunodeficiency-osteopetrosis-lymphedema syndrome

    Cholestasis-lymphedema syndrome

    Dahlberg-Borer-Newcomer syndrome

    Deafness-lymphedema-leukemia syndrome

    Genetic primary lymphedema

    Hennekam syndrome

    Hypotrichosis-lymphedema-telangiectasia-renal defect syndrome

    Lymphedema

    Lymphedema-atrial septal defects-facial changes syndrome

    Lymphedema-cerebral arteriovenous anomaly syndrome

    Lymphedema-distichiasis syndrome

    Lymphedema-posterior choanal atresia syndrome

    Macrothrombocytopenia-lymphedema-developmental delay-facial dysmorphism-camptodactyly syndrome

    Meige disease

    Microcephaly-lymphedema-chorioretinopathy syndrome

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    Monosomy 22q13

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    Noonan syndrome

    Noonan syndrome and Noonan-related syndrome

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    Noonan syndrome-like disorder with juvenile myelomonocytic leukemia

    Noonan syndrome-like disorder with loose anagen hair

    Primary lymphedema

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    Segmental progressive overgrowth syndrome with fibroadipose hyperplasia

    Syndromic lymphedema

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    Vascular Anomalies

    Arteriovenous malformation

    Blue Rubber Bleb Nevus syndrome

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    Diffuse neonatal hemangiomatosis

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    Generalized lymphatic anomaly

    Glomuvenous malformation

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    Infantile hemangioma of rare localization

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    Macrocystic lymphatic malformation

    Maffucci syndrome

    Megalencephaly-capillary malformation-polymicrogyria syndrome

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    Non-involuting congenital hemangioma

    Parkes-Weber syndrome

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    Primary intralymphatic angioendothelioma

    Proteus syndrome

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    Pulmonary arteriovenous malformation

    Rapidly involuting congenital hemangioma

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    Spindle cell hemangioma

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    CADASIL

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    Don't miss this informative and interactive webinar, that will take place on Monday, May 31st at 6pm (CET), with members of the Hereditary Haemorrhagic Telangiectasia Working Group (HHT-WG): Dr. Hans-Jurgen Mager, Prof. Marco Post, Claudia Crocione (ePAG Co-Chair for HHT) and Christina Grabowski (ePAG Deputy Co-Chair for HHT)!
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  • Recent Posts

    • Professor Miikka Vikkula was selected as the 2023 Earl P. Benditt Award Recipient!
    • Research News: A PPL WG audit of patients with pediatric and primary lymphedema
    • VASCERN Spotlights: Dr. Birutė Vaišnytė
    • Meeting in Oporto Portugal
    • New Guidelines for the Diagnosis and Management of Aortic Disease by the American College of Cardiology and American Heart Association
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