Clinical geneticist
VASCERN HTAD and MSA European Reference Centre
Center of Medical Genetics, University Hospital of Antwerp University of Antwerp
Upcoming
-
Fri18Jun20218:30AM-12:30PM (CET)
-
Mon21Jun20215:30PM-6:30PM (CET)
-
Wed23Jun2021
-
Rare diseases covered by VASCERN
Anhidrotic ectodermal dysplasia-immunodeficiency-osteopetrosis-lymphedema syndrome
Cholestasis-lymphedema syndrome
Dahlberg-Borer-Newcomer syndrome
Deafness-lymphedema-leukemia syndrome
Hypotrichosis-lymphedema-telangiectasia-renal defect syndrome
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
Microcephaly-lymphedema-chorioretinopathy syndrome
Non-hereditary late-onset primary lymphedema
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 with associated anomalies
Segmental progressive overgrowth syndrome with fibroadipose hyperplasia
Blue Rubber Bleb Nevus syndrome
Capillary malformation-arteriovenous malformation
Cerebral arteriovenous malformation
Cutis Marmorata Telangiectatica Congenita
Diffuse neonatal hemangiomatosis
Facial arteriovenous malformation
Familial cerebral cavernous malformation
Infantile hemangioma of rare localization
Kaposiform hemangioendothelioma
Klippel-Trรฉnaunay-Weber syndrome
Macrocystic lymphatic malformation
Megalencephaly-capillary malformation-polymicrogyria syndrome
Microcystic lymphatic malformation
Mixed cystic lymphatic malformation
Mucocutaneous venous malformation
Non-involuting congenital hemangioma
Partially-involuting congenital hemangioma
Primary intralymphatic angioendothelioma
Pulmonary arteriovenous malformation
Follow us on twitter
Like Us On Facebook
-
Recent Posts
- Recording of the VASCERN webinar: HHT and the lungs now available!
- Research News: Identification of new disease gene that plays key role in development of the aortic aneurysms
- Report from the Heritable Thoracic Aortic Diseases Working Group (HTAD WG)’s Virtual Spring Meeting
- Review of the Vascular Anomalies Working Groupโs 2-day Virtual Spring Meeting!
- Recap of the Pediatric and Primary Lymphedema Working Group (PPL WG)’s Virtual Spring Meeting!