Skin fragility syndrome
Skin Fragility Syndrome | |
---|---|
Other names | Epidermolysis Bullosa Simplex, Dermatolysis, etc. |
Skin Fragility Syndrome (SFS) encompasses a group of rare genetic disorders that result in easy blistering of the skin and mucous membranes in response to minor trauma or friction. The conditions are generally classified based on the specific layer of skin affected and can range in severity from mild to life-threatening. The most common types include Epidermolysis Bullosa Simplex (EBS), Dystrophic Epidermolysis Bullosa (DEB), Junctional Epidermolysis Bullosa (JEB), and Kindler Syndrome.
Causes[edit | edit source]
Skin Fragility Syndrome is primarily caused by genetic mutations that affect the proteins necessary for the integrity and stability of skin structure. These proteins include keratins (in EBS), collagen (in DEB), and laminins (in JEB). The mutations can be inherited in an autosomal dominant or recessive manner, depending on the type of SFS.
Symptoms[edit | edit source]
The hallmark symptom of SFS is the formation of blisters and sores on the skin and mucous membranes due to minor mechanical trauma. Other symptoms may include:
- Nail dystrophy or loss
- Scarring
- Mucosal involvement leading to dietary and respiratory issues
- In severe cases, systemic involvement such as growth retardation and anemia
Diagnosis[edit | edit source]
Diagnosis of SFS is based on:
- Clinical examination
- Family history
- Skin biopsy for histological examination
- Genetic testing to identify specific mutations
Treatment[edit | edit source]
There is currently no cure for Skin Fragility Syndrome. Treatment focuses on managing symptoms and preventing complications. This may include:
- Wound care and infection prevention
- Pain management
- Nutritional support
- Physical and occupational therapy
- Use of protective bandages and clothing to minimize trauma
- Surgical interventions for severe complications
Prognosis[edit | edit source]
The prognosis for individuals with SFS varies widely depending on the type and severity of the disorder. While some individuals may lead relatively normal lives with minor adjustments, others may suffer from severe and disabling complications.
See also[edit | edit source]
References[edit | edit source]
External links[edit | edit source]
- Dystrophic Epidermolysis Bullosa Research Association (DEBRA)
- National Institute of Arthritis and Musculoskeletal and Skin Diseases - Epidermolysis Bullosa
Skin fragility syndrome Resources | |
---|---|
|
Search WikiMD
Ad.Tired of being Overweight? Try W8MD's physician weight loss program.
Semaglutide (Ozempic / Wegovy and Tirzepatide (Mounjaro / Zepbound) available.
Advertise on WikiMD
WikiMD's Wellness Encyclopedia |
Let Food Be Thy Medicine Medicine Thy Food - Hippocrates |
Translate this page: - East Asian
中文,
日本,
한국어,
South Asian
हिन्दी,
தமிழ்,
తెలుగు,
Urdu,
ಕನ್ನಡ,
Southeast Asian
Indonesian,
Vietnamese,
Thai,
မြန်မာဘာသာ,
বাংলা
European
español,
Deutsch,
français,
Greek,
português do Brasil,
polski,
română,
русский,
Nederlands,
norsk,
svenska,
suomi,
Italian
Middle Eastern & African
عربى,
Turkish,
Persian,
Hebrew,
Afrikaans,
isiZulu,
Kiswahili,
Other
Bulgarian,
Hungarian,
Czech,
Swedish,
മലയാളം,
मराठी,
ਪੰਜਾਬੀ,
ગુજરાતી,
Portuguese,
Ukrainian
WikiMD is not a substitute for professional medical advice. See full disclaimer.
Credits:Most images are courtesy of Wikimedia commons, and templates Wikipedia, licensed under CC BY SA or similar.
Contributors: Prab R. Tumpati, MD