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Alopecia patients have more mast cells in their scalps, especially in severe cases and older age, with alopecia areata showing the highest increase.

The optimized chia seed oil hair serum is stable and meets all physical requirements.

The optimal pomegranate leaf extract shampoo formula effectively combats dandruff without causing hair loss.

Lichen simplex chronicus on the scalp can be diagnosed by specific hair and skin signs and treated with corticosteroids and therapy.

The study found different absorbance values for simplex and complex homoeopathic hair oils when analyzed with a UV-visible spectrophotometer.

Chronic bacterial infections of hair follicles can cause ongoing skin inflammation.

Mutations in the LSS gene cause a rare type of hereditary 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 new genetic area linked to a rare hair loss condition was found on chromosome 13 in a Chinese family.

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.

A specific gene mutation causes a rare hair loss condition in a Chinese patient.

The document's conclusion cannot be provided because the document is not available or cannot be understood.

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

Two siblings were found to have a genetic condition causing progressive hair loss and woolly hair, which may often be misdiagnosed.

Isotretinoin may effectively treat hereditary hypotrichosis simplex, a rare hair loss condition.

Scientists used stem cells to create a model of the skin disease Epidermolysis Bullosa simplex, which helped them understand its molecular mechanisms and could aid in finding treatments.

Combining PRP injections with minoxidil 2% effectively promotes hair growth in hereditary hair loss.

Oral minoxidil and growth factors improved hair density and thickness in a girl with hereditary hair loss.

The document concludes that a woman has both Frontal Fibrosing Alopecia and Lichen Simplex Chronicus, a previously unreported combination of conditions.

A boy and his father with hereditary hypotrichosis simplex were treated for hair loss, but the treatment result is unknown.

Black dots under trichoscopy can appear in different hair and scalp conditions, not just in alopecia areata.

The research suggests that a specific skin gene can be controlled by signals within and between cells and is wrongly activated in certain skin diseases.

Emotional factors are crucial in treating and preventing scalp neurodermatitis and hair loss.

Triple horizontal scalp biopsies are 98% accurate in diagnosing hair loss, better than single biopsies.

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

Researchers made a mouse model with curly hair and hair loss by editing a gene.

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

Hypertrichosis causes excessive hair growth and needs psychological support due to its impact on self-esteem.