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ECM changes may play a role in hair loss, with differences between males and females.

Multi-omics techniques help understand the molecular causes of androgenetic alopecia.

iPSCs show promise for hair regeneration but need more research to improve reliability and effectiveness.

Effective treatment guidelines for frontal fibrosing alopecia are still unclear.

A rare skin tumor with bone formation was successfully removed without recurrence.

Hair loss in Androgenetic Alopecia is caused by genetics, aging, and lifestyle, leading to hair follicle shrinkage and related health risks.

Skin cells and certain hair follicle areas produce hemoglobin, which may help protect against oxidative stress like UV damage.

Trichoscopic features help diagnose and assess female pattern hair loss severity, with inflammation playing a key role.

Younger people are at a higher risk for Fibrosing Alopecia in a Pattern Distribution than previously thought, with common symptoms and possible involvement of mast cells in its development.

Imiquimod can cause rare skin side effects, some irreversible, and long-term follow-up is important for users.

A scalp biopsy is essential for accurately identifying different types of hair loss.

RCM and OCT are effective for diagnosing and monitoring hair-related skin diseases but lack standardized protocols and need more research.

Reducing immunosuppression and using antiviral creams improved the woman's skin condition.

Isotretinoin effectively treated a rare scalp condition, but careful drug monitoring and a dairy-free diet were important.

Scarring alopecia, a type of hair loss, is most common in females under 35, often caused by discoid lupus erythematosus and pseudopelade of Brocq. Skin punch biopsy and histopathology are key to identifying its cause.

The document concludes that different types of permanent hair loss conditions are related and early treatment is key to preventing further damage.

An elderly woman with cancer improved after treatment for a rare skin condition with coiled hairs.

The research found that male pattern hair loss is mostly genetic and involves hair thinning due to hormonal effects and changes in gene expression.

The combined treatment for hair loss is effective, easy to use, and has mild side effects.

Androgenetic alopecia causes hair thinning due to increased androgen activity, treatable with minoxidil and finasteride.

The 'Swiss cheese' pattern in scalp biopsies can indicate trichotillomania, not just alopecia areata.

The microemulsion delivered the dye deeper into the skin than the cream.

Reflectance confocal microscopy confirms that yellow dots are signs of damaged hair follicles in alopecia areata.

Yellow dots in hair and scalp examinations are important for diagnosing different scalp conditions.

The document concludes that different patterns of hair thickness and scalp changes can help diagnose types of non-scarring hair loss.

A 15-year-old with KID syndrome developed a rare skin condition called PEHFN.

A new mutation in the hairless gene causes hair loss and skin wrinkling in mice.

The study concluded that a 'Swiss cheese' pattern in hair follicles is a useful sign for diagnosing alopecia areata.

Mice with a Gsdma3 gene mutation have thicker skin and longer hair follicle openings due to increased β-catenin levels.

A man with follicular psoriasis got better after treatment with skin cream and allergy pills.