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The document concludes that early diagnosis and treatment are crucial for managing skin diseases in ferrets.

Segmental Vitiligo is a stable, early-onset form of vitiligo that responds well to early treatment and is ideal for repigmentation studies.

A new gene variant in the DSP gene is linked to a unique type of hair loss.

Older adults often have skin problems due to aging, and treating these conditions requires attention to both physical and mental health.

Skin symptoms are important for diagnosing infections in children.

A 15-year-old girl has a skin condition causing blisters on her feet, likely inherited from her family.

Nonpalmoplantar skin cells can be made to express keratin 9 by interacting with palmoplantar fibroblasts.

A new keratin, hK6irs1, is found in all layers of the hair follicle's inner root sheath.

The project created a standardized system for classifying skin lesions in lab rats and mice.

Buffalo flies and Stephanofilaria nematodes cause severe skin lesions in beef cattle, and treatment should target both.

A specific gene variant is linked to heart disease, increased heart muscle, curly hair, and thick skin on palms and soles.

Early baldness in men may indicate risks for obesity, metabolic syndrome, insulin resistance, and heart disease, similar to women with PCOS. Alopecia areata is often linked with autoimmune diseases and mental health issues. Certain hair disorders are due to genetic issues, and chemotherapy can cause hair loss through specific biological pathways. Iron deficiency's link to hair loss is still disputed.

The man has a genetic skin condition called pachyonychia congenita.

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.

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

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

A rare gene mutation causes skin fragility and itching without affecting hair or nails.

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.

Most Recessive Dystrophic Epidermolysis Bullosa patients with a specific mutation likely have Sephardic ancestry from about 500 years ago.

Henna ointment may help reduce itching and improve wound healing in patients with epidermolysis bullosa.