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Mutations in the AP1B1 gene cause a new syndrome with skin, hearing, and developmental issues.

Keratosis Pilaris Atrophicans causes skin scarring and might be treated with a new synthetic retinoid.

Chemotherapy improved a girl's painful foot condition linked to pachyonychia congenita.

Keratoacanthoma changes as it grows, showing different hair follicle characteristics at each stage.

A benign skin tumor grew quickly in a dialysis patient and was surgically removed.

BKN-1 antibody targets specific keratin in basal cell epithelioma and normal skin basal cells.

A rare skin reaction from cancer treatment was successfully managed with topical treatments and antihistamines.

Keratosis pilaris is common in young females, and dermoscopy helps diagnose it accurately.

Keratoacanthomas and squamous cell carcinomas have similar keratin patterns, making them hard to tell apart.

RSPO1 mutations in certain patients lead to skin cells that don't develop properly and are more likely to become invasive, increasing the risk of skin cancer.

Tumor cells in calcifying epithelioma of Malherbe resemble hair follicle cells.

A baby boy with 13q deletion syndrome had eye cancer, a woman's vision improved after stopping a breast cancer drug, a man developed cataracts from using Propecia, and a rare skin disorder called Lipoid Proteinosis was discussed. Also, a tool called OCT is useful for diagnosing macular diseases.

Porokeratosis should be considered for scalp lesions, with new treatments like topical cholesterol/lovastatin offering promise.

RAPK is a rare skin disorder with pigmented spots, mainly on hands and feet, starting in youth.

A new mutation in the K6b gene caused a girl's late-appearing nail condition.

Substance P may play a role in the inflammation seen in keratosis follicularis spinulosa decalvans.

Nilotinib can cause generalized keratosis pilaris.

Keratin mutations cause skin diseases and could lead to new treatments.

High ODC and low K1 and K10 may indicate early skin tumors in mice.

Accurate diagnosis of APL is crucial to avoid unnecessary treatments.

Kerion is a rare but serious scalp infection that needs proper treatment.

Eyebrow reconstruction using hair follicle grafts was successful in a man with a benign hereditary disorder affecting his eyebrows.

Follicular porokeratosis may be linked to diabetes and can lead to hair loss.

A new type of pachyonychia congenita may exist, caused by a different keratin mutation.

The man has a genetic skin condition called pachyonychia congenita.

Mutations in hKAP1 genes may cause hereditary hair disorders.

Mutations in keratin genes cause skin disorders, but new treatments show promise.