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Skin cells and immune cells change in a skin condition called hidradenitis suppurativa, and a certain treatment can improve these changes.

Some burn patients grew extra hair in areas treated with pressure garments or silicone.

A new mutation in the hHb1 keratin gene is linked to the hair disorder monilethrix.

A wide range of proteins are integrated into the skin's protective layer.

A 2-year-old girl had a hair disorder not shared by her identical twin.

A new mouse gene, Keratin 17n, is mainly found in nail tissue and may explain why mice without Keratin 17 don't have nail issues.

CYLD deficiency in skin tumors disrupts hair follicle cell processes and protein secretion.

Topical minoxidil may help treat a rare genetic hair condition with no fully effective treatments yet.

KLF4 is important for keeping hair follicle stem cells inactive.

The protein aPKCλ is crucial for keeping hair follicle stem cells inactive and for hair growth and regeneration.

Dermoscopy helped correctly diagnose a skin condition that was previously misidentified as a different hair loss disease.

Regulating keratinocyte growth in engineered skin can improve wound healing.

Keratin K80 is an ancient protein found in various tissues, important for cell structure and tissue differentiation.

Mutations in keratin genes cause skin, hair, and nail disorders, with future treatments possible.

HHK can help restore skin structure.

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.

Kerion is a severe scalp infection that needs quick treatment to avoid permanent hair loss in children.

Dermoscopy is useful for diagnosing Atrichia with Papular Lesions in children without needing a biopsy.

A 16-year-old boy's arm hair grew more after wearing a splint, but it returned to normal in 8 months.

Inverted follicular keratosis can look like cancer but is actually a harmless tumor.

A family got a fungal infection from a boy who had contact with rabbits, but they all recovered with treatment.

The young woman has a benign, hereditary skin condition with no signs of a more serious syndrome.

A different gene near the hairless gene on chromosome 8p21 causes a rare hair loss condition in a German family.

Two genetic disorders affect biotin metabolism, causing severe skin, hair, and metabolic issues.

Trichoscopy helps accurately diagnose Netherton syndrome, often mistaken for atopic dermatitis.

Mutations in the desmoplakin gene can cause hair problems and deadly heart disease.

A new technique effectively treats and diagnoses eruptive vellus hair cysts without recurrence.

Trichoscopy is a helpful tool for diagnosing Netherton syndrome.