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(Q82.4) Ectodermal dysplasia (anhidrotic)
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266 982 in individuals diagnosis ectodermal dysplasia (anhidrotic) confirmed
2 472 deaths with diagnosis ectodermal dysplasia (anhidrotic)
1% mortality rate associated with the disease ectodermal dysplasia (anhidrotic)
Diagnosis ectodermal dysplasia (anhidrotic) is diagnosed Women are 6.25% more likely than Men
125 148
Men receive the diagnosis ectodermal dysplasia (anhidrotic)
1 374 (1.1 %)Died from this diagnosis.
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141 834
Women receive the diagnosis ectodermal dysplasia (anhidrotic)
1 098 (0.8 %)Died from this diagnosis.
Risk Group for the Disease ectodermal dysplasia (anhidrotic) - 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 90-94
In Women diagnosis is most often set at age 0-89, 95+
Disease Features ectodermal dysplasia (anhidrotic)
Absence or low individual and public risk
Ectodermal dysplasia (anhidrotic) - what does this mean
Ectodermal dysplasia (anhidrotic) is a genetic condition that affects the development of the skin, hair, nails, and sweat glands. it is caused by a mutation in the genes responsible for the development of these structures, resulting in abnormal development and a lack of sweat glands, which leads to decreased ability to regulate body temperature.
What happens during the disease - ectodermal dysplasia (anhidrotic)
The best way to prevent ectodermal dysplasia (anhidrotic) is to maintain a healthy lifestyle. This includes eating a balanced diet, exercising regularly, avoiding smoking and alcohol, and getting adequate sleep. Additionally, it is important to practice good hygiene, such as washing hands frequently and avoiding contact with people who are sick. Vaccines are also important in preventing some forms of ectodermal dysplasia. It is important to consult with a doctor or medical professional to determine the best course of action for prevention.
Clinical Pattern
Ectodermal dysplasia (anhidrotic) is a rare genetic disorder characterized by the abnormal development of the skin, hair, nails, teeth, and sweat glands. Symptoms may include sparse scalp and body hair, dry skin, absent or malformed teeth, and the inability to sweat. It is caused by mutations in genes related to the development of ectodermal tissues. Treatment typically includes the use of topical moisturizers, antibiotics, and dental implants.
How does a doctor diagnose
- Physical examination to assess the presence of ectodermal dysplasia (anhidrotic) symptoms
- Genetic testing to confirm the diagnosis
- Skin biopsy to assess the presence of abnormal skin cells
- Blood tests to check for electrolyte imbalances
- X-rays to look for any skeletal abnormalities
Treatment and Medical Assistance
Main goal of the treatment: To improve the patient's quality of life by reducing the symptoms of ectodermal dysplasia (anhidrotic).
- Provide adequate hydration and nutrition to the patient
- Encourage the use of humidifiers and other skin care products to keep the skin hydrated
- Prescribe oral medications for pain relief
- Prescribe topical medications to reduce skin inflammation and itching
- Prescribe antibiotics to treat any infections
- Refer the patient to a dermatologist for specialized care
- Refer the patient to a genetic counselor for genetic counseling
- Provide counseling and support to the patient and their family
8 Days of Hospitalization Required
69 Hours Required for Outpatient Treatment
Ectodermal dysplasia (anhidrotic) - Prevention
Ectodermal dysplasia (anhidrotic) can be prevented by avoiding environmental exposures, such as smoking, alcohol, and certain chemicals, which can increase the risk of developing the disorder. additionally, genetic counseling should be sought for those with a family history of the disorder.