DocSym
β
Searchsearch
Search
(Q79.6) Ehlers-danlos syndrome
More details coming soon
203 021 in individuals diagnosis ehlers-danlos syndrome confirmed
13 891 deaths with diagnosis ehlers-danlos syndrome
7% mortality rate associated with the disease ehlers-danlos syndrome
Diagnosis ehlers-danlos syndrome is diagnosed Men are 2.86% more likely than Women
104 416
Men receive the diagnosis ehlers-danlos syndrome
7 358 (7.0 %)Died from this diagnosis.
100
95
90
85
80
75
70
65
60
55
50
45
40
35
30
25
20
15
10
5
0
98 605
Women receive the diagnosis ehlers-danlos syndrome
6 533 (6.6 %)Died from this diagnosis.
Risk Group for the Disease ehlers-danlos syndrome - Men and Women aged 0
In Men diagnosis is most often set at age 0-89
Less common in men the disease occurs at Age 90-95+Less common in women the disease occurs at Age 95+
In Women diagnosis is most often set at age 0-94
Disease Features ehlers-danlos syndrome
Absence or low individual and public risk
Ehlers-danlos syndrome - what does this mean
Ehlers-danlos syndrome is a group of inherited disorders caused by a defect in the structure, production, or processing of collagen, a protein that provides strength and elasticity to connective tissues such as skin, ligaments, and blood vessels. this defect can lead to joint hypermobility, skin hyperextensibility, and tissue fragility.
What happens during the disease - ehlers-danlos syndrome
Ehlers-danlos syndrome is caused by a genetic defect in the production of collagen, a protein that provides structure and strength to connective tissues such as skin, ligaments, and tendons. this defect can affect the strength and stability of these tissues, leading to joint hypermobility, skin fragility, and tissue fragility. in some cases, the defect can also affect the strength of blood vessels, leading to an increased risk of arterial or organ rupture.
Clinical Pattern
More details coming soon
How does a doctor diagnose
- Physical examination
- Blood tests
- Genetic testing
- Skin biopsy
- MRI scan
- Ultrasound
- CT scan
- Joint X-rays
- Electrocardiogram (ECG)
Treatment and Medical Assistance
Main goal of the treatment: Improve the quality of life of people with Ehlers-Danlos syndrome.
- Physical therapy to improve mobility and reduce pain
- Occupational therapy to help with daily activities
- Pain management
- Counseling and support groups
- Medications to reduce inflammation and pain
- Surgery to correct joint dislocations
- Regular check-ups with a doctor
- Regular monitoring of heart and joint health
- Regular exercise and stretching
- Proper nutrition and hydration
- Avoidance of activities that may cause injury
25 Days of Hospitalization Required
Average Time for Outpatient Care Not Established
Ehlers-danlos syndrome - Prevention
Ehlers-danlos syndrome is a genetic disorder that affects the body's connective tissues. prevention of this disorder is not possible, however, early diagnosis and proper management of the condition can help to reduce the severity of the symptoms and prevent complications. it is important to seek medical attention if any symptoms of ehlers-danlos syndrome are present, as early diagnosis and treatment can help to reduce the risk of complications.