Submit a case
Home - About VASCERN - Structure and Governance - Working Groups - Rare Disease Working Groups - Heritable Thoracic Aortic Diseases (HTAD-WG) - Diseases Covered
Heritable Thoracic Aortic Diseases (HTAD-WG)
Introduction Diseases Covered
Experts & Centers
Experts Centers
Clinical Decision Support Tools
Patient Pathways Do’s and Don’ts Clinical Practice Guidelines (CPGs) adopted Clinical Expert Consensus Statements Written Outcome Measures
Registry
Research
Clinical Trials/Observational Studies Research Publications
Training and Education
E-Learning Pills of Knowledge (PoK) Webinars
Sub Working Groups
Aortic Imaging Gene Compendium
Pediatrics
Members
Variants

Diseases Covered

Heritable Thoracic Aortic Disease (HTAD) covers disease entities with as common denominator Thoracic aortic aneurysms or – dissections that are familial and/or caused by genetic defects. Both syndromic and nonsyndromic entities exist. Although the number of genes involved in HTAD is steadily increasing, a large number of patients/families with HTAD have no identifiable defect, indicating that other genes must be involved. Genetic defects identified so far have can be categorized  into (1) genes encoding components of the extracellular matrix (FBN1, MFAP5, MAT2A); (2) genes encoding components of the TGFbeta signaling pathway (TGFBR1/2, TGFB2/3, SMAD2/3); (3) genes encoding components of the smooth muscle cell contractile apparatus (ACTA2, MYH11, MYLK, PRKG1). Clinical entities covered by this WG include:

  • syndromic entities such as Marfan Syndrome (ORPHA558), Loeys Dietz Syndrome (ORPHA60030), Aneurysm Osteoarthritis syndrome (ORPHA284984), Arterial tortuosity syndrome (ORPHA3342), Multisystemic smooth muscle dysfunction syndrome (ORPHA404463) and Neonatal Marfan syndrome (ORPHA284979)
  • As well as nonsyndromic entities such as Familial Thoracic Aortic Aneurysms Dissections (Familial TAAD) (ORPHA91387), Familial aortic dissection (ORPHA229),
  • caused by pathogenic variants in
    • actin, alpha 2, smooth muscle, aorta – ACTA2
    • fibrillin 1 – FBN1
    • microfibrillar associated protein 5 – MFAP5
    • myosin, heavy chain 11, smooth muscle – MYH11
    • myosin light chain kinase – MYLK
    • protein kinase, cGMP-dependent, type I – PRKG1
    • SMAD family member 3 – SMAD3
    • SMAD family member 2 -SMAD2
    • transforming growth factor beta 2 – TGFB2
    • transforming growth factor beta 3 – TGFB3
    • transforming growth factor beta receptor I – TGFBR1
    • transforming growth factor beta receptor II – TGFBR2

For more information on the various diseases – click here

While our knowledge of clinical and genetic characteristics of MFS and related HTAD has increased substantially, already resulting in a better outcome in these patients, further efforts are needed to improve management and increase awareness of these rare disorders since knowledge of the disease appears to be the most important factor influencing outcome. Next stages require formal acknowledgement, status and funding to ensure personalised medicine and therapeutics.

Bases for the following estimated incidence and prevalence numbers: 500 Million inhabitants within European union with about 6 million newborns annually.

Sub-thematic areas of expertise Rare of complex disease(s) or condition(s) or highly specialized interventions Code/ICD/Orphacode/Group of codes Incidence (Number of cases/year) (in the EU) Prevalence (in the EU)
HTAD Aneurysm-Osteoarthritis Syndrome ICD 10: 171, ORPHA284984 60 5000
HTAD Arterial Tortuosity Syndrome ICD 10: 171, ORPHA3342 unknown unknown
HTAD Familial bicuspid aortic valve ICD 10: 171, ORPHA402075 unknown unknown
HTAD Familial thoracic aortic aneurysm and aortic dissection ICD 10: 171, ORPHA91387 1200 100000
HTAD Loeys Dietz Syndrome ICD 10: 171, ORPHA60030 180 15000
HTAD Marfan Syndrome ICD 10: 171, ORPHA558 3300 150000
HTAD Multisystemic smooth muscle dysfunction syndrome ICD 10: 173, ORPHA404463
HTAD Rare disease with thoracic aortic aneurysm and aortic dissection ICD 10: 171, ORPHA285014 unknown unknown
Skip to content