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Protein kinase C epsilon may promote skin cancer development after UV exposure by affecting nearby cells.

A 21-year-old with lichen planopilaris was successfully treated, stopping disease progression and preventing crusts.

Keratin-associated protein nanoparticles from human hair may help stop bleeding quickly and safely.

A woman developed a skin condition called Pemphigus Vulgaris after a treatment to help with hair loss.

An 8-year-old girl has a rare, irreversible hair loss condition caused by a genetic mutation.

A boy with chromosome 13q deletion syndrome developed eye cancer, a woman with breast cancer lost vision due to a rare side-effect of her treatment, a man's vision worsened after using a hair loss drug, and two rare disorders were discussed. Optical Coherence Tomography is useful for diagnosing and monitoring these conditions.

Restoring phenylalanine levels improved skin and hair symptoms in a PKU infant.

Sheep with chronic Sarcoptes scabiei dermatitis have altered keratin expression in their skin.

A specific gene variant is linked to heart disease, increased heart muscle, curly hair, and thick skin on palms and soles.

PRP injections are safe for hair loss treatment, but monitoring and sun protection are advised.

Seborrheic keratosis shows varied cell differentiation, and keratin analysis helps diagnose skin tumors.

The virus linked to a rare disease was found in a patient's blood and urine before skin symptoms appeared.

Fetal skin biopsy can help diagnose protein-related disorders before birth.

A rare genetic skin condition usually affecting males was found in a 9-year-old girl.

Keratin proteins are increasingly recognized as important for cell health and are linked to many diseases.

Erosive pustular dermatosis of the scalp can occur about 17 weeks after starting EGFR inhibitors, and early minocycline may help manage it.

A new gene mutation linked to KID syndrome was found, expanding genetic knowledge.

A mutation in the KRT71 gene causes a hair disorder by disrupting hair follicle structure and texture.

Seborrheic keratosis is a common, harmless skin growth that can look like cancer, so it may need a biopsy.

Dermoscopy is useful for diagnosing facial actinic keratosis by identifying specific skin patterns.

A new genetic mutation in the hairless gene causes a rare hair loss disorder.

Almost all patients with chronic kidney disease not yet on dialysis have at least one skin problem.

Pigmented papules on the ear can be a rare skin condition called cutaneous amyloidosis, treatable with topical tretinoin.

Blocking mTORC1 reduces skin tumor growth in mice.

Keratosis pilaris is a common skin condition where hair follicles get clogged with keratin, mostly on the arms and thighs.

Genetic testing for EGFR mutations is crucial in similar cases.

Polarizing light microscopy can easily and reliably diagnose congenital keratinizing disorders like Netherton syndrome.

Zouboulis syndrome is a rare condition that helps diagnose monosomy 18p early.