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A patient with a PLEC mutation has epidermolysis bullosa, muscular dystrophy, and myasthenia gravis, which improved with steroid treatment.

Neutrophils quickly respond to skin injury.

A 37-year-old male with severe skin and internal issues has a rare inherited skin condition called dystrophic epidermolysis bullosa.

Alopecia in patients with epidermolysis bullosa varies in severity and is often caused by skin blistering or trauma.

The document is a detailed medical reference on skin and genetic disorders.

Lichen Planopilaris is a hair loss condition best treated early with various medications, including hydroxychloroquine, to prevent permanent baldness.

No effective treatment for frontal fibrosing alopecia was found, but oral 5-alpha-reductase inhibitors had the best response; for lichen planopilaris, topical corticosteroids were commonly used but had a high relapse rate.

Dupilumab is being tested for many new skin, respiratory, and gastrointestinal conditions.

The document concludes that inherited epidermolysis bullosa is a challenging genetic condition requiring multidisciplinary care and new treatments.

The document suggests that certain protein deficiencies and scalp blistering in Epidermolysis Bullosa may cause hair loss.

The document is a detailed guide on skin conditions and treatments for dermatologists.

The document suggests a bacteria plays a significant role in acne rosacea and that white hair can regain color after transplant, meriting more research on reversing grey hair.

There are still challenges in diagnosing and treating chronic skin diseases, but there is hope for future improvements.

Colchicine might help treat different skin diseases, but more research is needed to confirm its effectiveness and safe dosage.

The conclusion is that early diagnosis of skin signs linked to diseases like Lupus, Dermatomyositis, and Rheumatoid Arthritis is crucial to prevent serious complications.

Epidermolysis bullosa simplex causes easily blistered skin due to faulty skin cell proteins, leading to new treatment ideas.

Three new types of a skin blistering disease were found, caused by specific gene mutations.

Epidermolysis bullosa is a genetic disease causing fragile skin and blisters in both animals and humans.

A new mutation in the PLEC gene causes a rare condition with skin blistering, muscle weakness, and hair loss.

A 6-year-old boy's skin condition improved after stopping a specific treatment and starting new medications.

Colored hair-thickening fibers can help hide hair loss in some people with Epidermolysis Bullosa but may cause scalp irritation.

Skin cells from people with Epidermolysis Bullosa Simplex have abnormally placed and less active mitochondria.

The p.P25L mutation in the KRT5 gene causes a rare skin condition that worsens over time and may lead to hair loss starting in young adulthood.

Two patients with the same genetic mutation had both blistering skin and easily pulled out hair.

People with Epidermolysis bullosa have many health problems including poor oral health, which is often neglected due to other medical issues.

A patient with a rare hair condition and skin disorder showed hair improvement after treatment.

Middle Eastern patients with epidermolysis bullosa show specific genetic mutations linked to different types of the disease.

The specific skin disease variant p.(Arg2000Trp) in plectin can cause a wide range of symptoms, which should be considered when diagnosing patients.

Epidermolysis bullosa is an inherited condition causing fragile skin with no cure, managed by wound care and experimental treatments show promise.