Takayasu Arteritis
Description
Takayasu arteritis (TAK) is a rare inflammatory large-vessel vasculitis primarily affecting the aorta and its major branches, but also other large vessels, causing stenosis, occlusion, or aneurysm.
Clinical Features
Top most frequent phenotypes and symptoms related to Takayasu Arteritis
- Seizures
- Muscle weakness
- Anemia
- Hypertension
- Fever
- Fatigue
- Dilatation
- Hyperhidrosis
- Weight loss
- Arthralgia
And another 31 symptoms. If you need more information about this disease we can help you.
Incidence and onset information
— Based on the latest data available TAKAYASU ARTERITIS have a estimated incidence of 0.19 per 100k worldwide.— No data available about the known clinical features onset.
Alternative names
Takayasu Arteritis Is also known as young female arteritis, aortic arch syndrome, pulseless disease.
Researches and researchers
Doctors, researchs, and experts related to Takayasu Arteritis extracted from public data.
Takayasu Arteritis Experts map
Current Researchs and researchers
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Coordinator of expert centre - Clinical expert - Principal investigator of clinical trial - Manager of registry - Contact person of registry - Coordinator of research networkPARIS — Pr Loïc GUILLEVIN
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Institution/s:
— CHU Paris Centre - Hôpital Cochin, Site Cochin -
Research area/topic::
GFEV: French study group on vasculitis - research organization on necrotising angeitis, systemic diseases and vaccinale research
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Institution/s:
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Investigator of research project - Manager of registryLÜBECK — Pr Wolfgang L. GROSS
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Institution/s:
— Universitätsklinikum Schleswig-Holstein - Campus Lübeck -
Research area/topic::
DCVAS: American College of Rheumatology/European League Against Rheumatism (ACR/EULAR) - Study to develop new diagnostic and classification criteria for Primary Systemic Vasculitis
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Institution/s:
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Principal investigator of clinical trial - Investigator of research projectBARCELONA — Dr María Cinta CID XUTGLA
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Institution/s:
— Hospital Clínic de Barcelona -
Research area/topic::
ACR/EULAR: endorsed study to develop new diagnostic and classification criteria for primary systemic vasculitis
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Institution/s:
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Coordinator of expert centre - Principal investigator of clinical trial - Investigator of clinical trial - Coordinator of research networkCAMBRIDGE — Dr David JAYNE
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Institution/s:
— Cambridge University Hospitals NHS Foundation Trust, Addenbrooke's Hospital -
Research area/topic::
EUVAS: European vasculitis study group
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Institution/s:
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Investigator of research projectCAMBRIDGE — Dr James PETERS
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Institution/s:
— University of Cambridge -
Research area/topic::
An integrated genetic and proteomic approach to understanding cardiovascular disease aetiology
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Institution/s:
Takayasu Arteritis Recommended genes panels
Panel Name, Specifity and genes Tested/covered |
---|
![]() By Cincinnati Children's Hospital Medical Center Laboratory of Genetics and Genomics Cincinnati Children's Hospital Medical Center (United States).
IL12B
Specificity
100 %
Genes
34 % |
![]() By CGC Genetics (Portugal).
IL12B
Specificity
100 %
Genes
34 % |
![]() By Centogene AG - the Rare Disease Company (Germany).
IL12B
Specificity
100 %
Genes
34 % |
![]() By CeGaT GmbH (Germany).
STAT1, TAZ, TCIRG1, TCN2, TERT, WAS, WIPF1, ACTB, VPS45, HPS3, HPS4, HAX1, HPS5, DTNBP1, CEBPE, HPS6, SBDS, SLC35C1, BLOC1S3, VPS13B , (...)
View the complete list with 39 more genes
Specificity
2 %
Genes
34 % |
![]() By Invitae (United States).
STAT1, STAT2, ACP5, TYK2, SAMHD1, IRAK4, ADAR, CYBB, ISG15, GATA2, IRF8, IFNGR1, IFNGR2, IL12B, IL12RB1, MYD88
Specificity
7 %
Genes
34 % |
![]() By Invitae (United States).
RMRP, RORC, SEMA3E, SH2D1A, SH3BP2, SLC7A7, SMARCAL1, BTK, STAT1, STAT2, STAT3, STAT5B, STIM1, STK4, STX11, STXBP2, TAPBP, TAZ, TBK1, TCN2 , (...)
View the complete list with 187 more genes
Specificity
1 %
Genes
34 % |
![]() By Fulgent Genetics Fulgent Genetics (United States).
IL12B
Specificity
100 %
Genes
34 % |
![]() By Blueprint Genetics (Finland).
RMRP, RORC, CFB, BLM, SH2D1A, SLC7A7, SMARCAL1, SMARCD2, SRP72, BTK, STAT1, STAT2, STAT3, STAT5B, STIM1, STK4, STX11, STXBP2, TAPBP, TBX1 , (...)
View the complete list with 253 more genes
Specificity
1 %
Genes
34 % |
You can get up to 0 more panels with our dedicated tool
Learn moreSources and references
You can check the following sources for additional information.
ORPHANET OMIM Rare Disease Symptoms CheckerIf you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE 5; DKCB5 FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 2; FSHD2 DYSKINESIA, FAMILIAL, WITH FACIAL MYOKYMIA; FDFM COXOPODOPATELLAR SYNDROME MENTAL RETARDATION, X-LINKED, WITH PANHYPOPITUITARISM NEUROBLASTOMA