Names |
- Morbus Adamandiades-Behçet
Category: Vascular system |
Prevalence |
Published: 17,332 cases in the US (Calamia 2009 and Mohammad 2013. ).
ARI Data: An estimated 52,255 cases in the U.S. Female/Male ratio: 2.5x. |
Age of Onset |
Onset typically occurs between ages 20 and 40. |
Description |
Behçet's syndrome is a chronic inflammatory disease that leads to mass inflammation in the blood vessels of the body which results in artery and vein damage. Many of the symptoms can seem unrelated at first, such as mouth sores, eye inflammation, skin rashes, etc, however, symptoms vary from person to person and varies depending on the body parts that are affected. Unfortunately, Behçet’s syndrome can lead to more serious complications such as blindness.
This disease is not well understood but is believed to be autoimmune in nature since the symptoms are due to vasculitis. Researchers have also found several genes to be associated with Behçet’s and believe that those with these genes can trigger Behçet’s if they are exposed to a virus or bacterium.
Evidence of autoimmunity: Antibody ICD-10 Code: M35.2     SNOMED Code: 310701003
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Symptoms |
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Resources |
Link to Clinical Trials Link to PubMed |
References |
Link to Cleveland Clinic
Link to Healthline
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Profile by: Autoimmune RegistryProfile updated September 2024Charts generated Feb 19, 2025 at 06:51 PM ET |
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Behcet's syndrome sex breakdown
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Behcet's syndrome age breakdown
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