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Scalp areas that look normal in people with hair loss may still show signs of disease under a microscope.

KIF18B is important for correctly positioning cell division machinery in skin cells, affecting hair follicle development.

LC-OCT can help identify lupus-related scarring hair loss by spotting unique features.

Human hair keratin has a 40% α-helix structure that changes to a random coil in 8 M urea.

Trichoscopy can help diagnose early congenital syphilis in newborns.

Scientists found a new protein, AMY117, common in Alzheimer's patients, which could be important for treatment and diagnosis.

Lichen planopilaris and frontal fibrosing alopecia are likely the same disease with different clinical appearances.

Pili anulati may cause hair loss, proper diagnosis and treatment needed.

Correcting EDA fibronectin organization and YAP translocation can improve wound healing in fibrotic conditions.

Diagnosing hair loss disorders needs clinical, dermoscopic, and histological differences, and checking menstrual cycle, weight changes, drug therapy, and nail changes.

Epidermal cysts come from the skin, while pilar cysts come from hair follicles.

Keratin proteins are consistent across different hair types from the same person.

The authors updated the criteria for diagnosing frontal fibrosing alopecia, making it easier to diagnose without a biopsy.

The study found specific proteins that could mark different growth stages of cashmere goat hair and may help improve cashmere production.

Monilethrix, a genetic hair disorder causing fragile hair, affects three generations in a family.

A simple wash test can help differentiate between two types of hair loss, and dermatoscopy should be used for further clarification.

Hair texture changes with age due to varying levels of lipids.

FFA patients have higher metal levels in hair, possibly linked to product use.

A unique hair tumor with a rippled pattern was identified, showing incomplete differentiation and unusual cell arrangements.

Horizontal sections of scalp biopsies are useful for telling the difference between Androgenetic Alopecia and Alopecia Areata.

Combining cell conditioning with mild protease digestion effectively shows versican mRNA in mouse skin sections.

A 4-year-old girl had a rare hair disorder affecting only part of her scalp.

Lack of small, fine hair on the front hairline is a key sign of frontal fibrosing alopecia.

HFMs can help study hair growth and test potential hair growth drugs.

Fibrosing alopecia in a pattern distribution is a unique hair loss condition with inflammation and scarring, resembling but distinct from common balding.

Frontal Fibrosing Alopecia is a type of hair loss that mainly affects postmenopausal women, has unclear causes, and lacks evidence-based treatments.

A new staining method shows a special area in the hair's skin layer with lots of proteoglycans.

Testing hair roots with a special dye is a simple, non-invasive way to check disease progress in pemphigus vulgaris patients.

Asian patients with Frontal Fibrosing Alopecia often lose eyebrow hair and respond well to combined antiandrogen or antimalarial and topical treatments.