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AS-OCT is crucial for diagnosing VZV interstitial keratitis and avoiding unnecessary treatments.

Some skin conditions in pets can signal cancer or may develop into cancer, and monitoring or treating these can help detect or manage the disease.

PRP shows promise for eye disease in animals but needs more research before being standard care.

Mutations in the KRT16 gene can cause skin and nail disorders.

Keratin-associated proteins are part of the developing hair fiber cuticle.

Recognizing scalp symptoms in PRP is crucial for proper diagnosis and treatment.

Keratin 15 cells from hair follicles help develop and maintain skin tumors in mice.

Scientists discovered a unique hair protein, KAP24.1, with a special structure, found only in the upper part of hair cuticles.

α-parvin is necessary for skin and hair growth and for the correct orientation of skin cells.

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.

Lichenoid keratosis can cause localized hair loss.

Ulerythema ophryogenes causes hair thinning and inflammation, with limited treatment options.

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

Onychopapilloma likely originates from the nail bed, not the nail matrix.

Intralesional therapy for keratoacanthoma is effective and has fewer side effects than systemic treatments.

Triptolide effectively and safely reduces actinic keratosis lesions in mice.

Poromas are related to sweat duct cells, and CK patterns help distinguish apocrine poromas from other neoplasms.

A man with KID syndrome developed a rare cancer in a long-term skin infection.

A rabbit gene important for hair development was identified and detailed.

Keratin gene mutations cause various skin and hair disorders, but new research offers hope for future treatments.

Keratin-75 is secreted by ameloblasts in a unique way without a signal peptide.

The report shows a young man with Hutchinson-Gilford Progeria Syndrome had typical and additional eye problems related to the disease.

Carriers of a specific gene mutation have subtle skin changes without visible symptoms.

Misdiagnosing kerion as a bacterial infection can lead to unnecessary surgery and permanent hair loss.

A man's skin condition and poor diet led to a scurvy diagnosis.

A young boy with a rare skin and nail condition improved significantly with simple topical treatments.