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The study found that tight junctions reach the top layer of the skin's stratum granulosum, not just the second top layer as previously thought.

A 72-year-old man was diagnosed with a rare skin form of Rosai-Dorfman disease after years of misdiagnosis.

Certain immune markers may predict chemotherapy response in mesothelioma, and nivolumab is a tolerable and effective treatment for advanced non-small cell lung cancer.

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Early intervention is important for limited systemic sclerosis patients due to higher pain and ulceration risks.

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Microarray analysis helps find hidden chromosomal changes in patients with intellectual disabilities and birth defects.

CD8+ T cells attack hair follicle stem cells, causing scarring and hair loss.

Prednisolone improved symptoms in a woman with Cronkhite-Canada syndrome, but regular screenings are needed due to cancer risk.

TCDD speeds up skin barrier formation by increasing certain gene expressions.

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Early diagnosis, genetic testing, and personalized care are essential for managing tuberous sclerosis.

Microbial biofilms may cause red scrotum syndrome.

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Some people with schwannomatosis have a new type of mutation in the LZTR1 gene.

Ichthyosis with confetti is a genetic skin disorder with consistent ectodermal malformations and various KRT10 gene mutations.

Scientists found a new gene in a bacterium that can modify an immunosuppressant drug, potentially helping to treat hair loss.

Cal/BD aerosol foam effectively treats scalp psoriasis, improving symptoms and patient satisfaction.

Strontium ranelate helps cartilage growth by blocking a specific cell pathway.

Patients with Complete Androgen Insensitivity Syndrome need psychological support and multidisciplinary care for complex treatment decisions.

A 70-year-old man with skin cancer on both sides of his forehead was treated with surgery and cryotherapy, highlighting the need for early detection and prevention.

A new 3D-printed hydrogel scaffold helps regenerate corneas and prevent scarring.

A rare case of Cushing's syndrome and pheochromocytoma requires careful re-evaluation to avoid complications.

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Mutations in the DSG4 gene can cause a rare hair disorder similar to monilethrix.

New mutations in the DSG4 gene cause a rare hair condition.