The EURORDIS BEST PRACTICE WEBINARS: Deep dive on integration of ERNs into national health systems will take place on October 14th at 2PM (CET).
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Hereditary haemorrhagic telangiectasia
Aneurysm Osteoarthritis Syndrome
Arterial Tortuosity Syndrome
Familial forms of bicuspid aortic valve with aortopathy
Familial thoracic aortic aneurysm and aortic dissection
Loeys Dietz Syndrome
Marfan Syndrome
Rare disease with thoracic aortic aneurysm and aortic dissection
Vascular Ehlers Danlos Syndrome
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
Milroy disease
Monosomy 22q13
Non-hereditary late-onset primary lymphedema
Noonan syndrome
Noonan syndrome and Noonan-related syndrome
Noonan syndrome with multiple lentigines
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia
Noonan syndrome-like disorder with loose anagen hair
Primary lymphedema
Primary lymphedema with associated anomalies
Segmental progressive overgrowth syndrome with fibroadipose hyperplasia
Syndromic lymphedema
Turner syndrome
Turner syndrome due to structural X chromosome anomalies
Yellow nail syndrome
Arteriovenous malformation
Blue Rubber Bleb Nevus syndrome
Capillary malformation-arteriovenous malformation
Cerebral arteriovenous malformation
CLAPO syndrome
CLOVES syndrome
Cutis Marmorata Telangiectatica Congenita
Diffuse neonatal hemangiomatosis
Facial arteriovenous malformation
Familial cerebral cavernous malformation
Generalized lymphatic anomaly
Glomuvenous malformation
Gorham-Stout syndrome
Infantile hemangioma of rare localization
Kaposiform hemangioendothelioma
Klippel-Trénaunay-Weber syndrome
LUMBAR association
Lymphatic malformation
Macrocystic lymphatic malformation
Maffucci syndrome
Megalencephaly-capillary malformation-polymicrogyria syndrome
Microcystic lymphatic malformation
Mixed cystic lymphatic malformation
Mucocutaneous venous malformation
Non-involuting congenital hemangioma
Parkes-Weber syndrome
Partially-involuting congenital hemangioma
PHACE association
Primary intralymphatic angioendothelioma
Proteus syndrome
PTEN hamartoma tumor syndrome
Pulmonary arteriovenous malformation
Rapidly involuting congenital hemangioma
Rare capillary malformation
SACRAL association
Spindle cell hemangioma
Sturge-Weber syndrome
Tufted angioma
Venous malformation
Verrucous hemangioma
CADASIL
Moyamoya disease
✨"What makes me the most proud is that I am now meeting the sons and daughters of my patients that I started treating when they were children. I have seen them grow up, overcome problems, get married, have children and lead normal lives, despite their rare disease – and this is a wonderful thing!" ✨Read the new VASCERN Spotlights article featuring Dr. Alessandro Pini from Italy! Dr. Pini is Chair of our eHealth Working Group and a member of both the Heritable Thoracic Aortic Diseases (HTAD) and Medium Sized Arteries (MSA) WGs. He shares his greatest hopes for our network and talks about VASCERN app and why he decided to dedicate himself to rare vascular diseases, in particular those affecting the aorta, which includes Marfan syndrome! Read the full article here➡: https://vascern.eu/vascern-spotlights-alessandro-pini/ Marfan Clinic Marfan Europe Network The Marfan Foundation AssoMarfans Association Belge du Syndrome de Marfan - ABSM asbl Marfan Hilfe - Deutschland e.V. Svenska Marfanföreningen ... See more