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Mutations in the LSS gene cause a rare type of hereditary hair loss.

Alfredo Rebora suggested a new, easier way to classify hair loss in Telogen Effluvium, adding a type possibly related to autoimmune diseases.

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.

Roselle flower extracts can protect against free radical damage in UV-irradiated antibiotics.

Zebrafish are useful for studying and developing treatments for human skin diseases.

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.

3D imaging of skin biopsies offers better accuracy but is time-consuming and can't clear melanin.

Using a wall mirror to design the hairline in hair restoration surgery is simple, cheap, and effective for natural-looking results.

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

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

The document provides a simple method for beginners to learn hair restoration surgery.

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.

Hair transplant surgeons should also focus on their patients' overall health, including regular check-ups and screening for common health issues.

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.

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

A stable and simple finasteride suspension was developed that retains over 94.3% of its concentration for up to 90 days and doesn't significantly increase occupational exposure, but safety measures are still advised.

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.

Light microscopy is useful for diagnosing different hair disorders.

The "Two-Cell Assemblage" assay is a new, simple method to identify substances that may promote hair growth.

The document concludes that understanding hair loss patterns and careful surgical techniques are key for successful hair transplantation in oral and maxillofacial surgery.

Method measures finasteride in plasma, suitable for pharmacokinetic studies.

A woman lost her hair after taking acyclovir, but it grew back when she stopped the medication.