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Chronic scalp lesions with crusts and pus that heal with strong topical steroids suggest Erosive Pustular Dermatosis, confirmed by biopsy showing specific immune cells.

Rituximab may be an effective treatment for Cronkhite-Canada syndrome with kidney disease.

Brodalumab is more effective than ustekinumab in treating psoriasis.

PKC ε increases hair follicle stem cell turnover and may raise skin cancer risk.

Some people with lichen planus pigmentosus might later develop frontal fibrosing alopecia.

Patients with chronic kidney disease often have various skin problems that affect their quality of life, but early treatment can help.

A new genetic change in the keratin 10 gene caused a skin condition called ichthyosis hystrix in a father and his daughter.

Papular acantholytic dyskeratosis of the vulva is a rare, benign skin condition that can be managed conservatively.

The study concluded that key signs of Keratosis follicularis spinulosa decalvans are changes in terminal hair and vellus hair follicles, which likely start the inflammation and damage to hair follicles.

Cathepsin E is crucial for normal skin cell differentiation and development.

Trichodysplasia spinulosa can occur after a heart transplant due to immunosuppressive drugs.

A 90-year-old woman's hand lesion was a rare, aggressive skin cancer treated successfully with surgery.

Advanced microscopy shows hair damage and keratin proteins' roles, aiding future cosmetic treatments.

Terbinafine effectively treated kerion celsi despite disrupted immune responses.

Cathepsin L deficiency causes hair and skin issues in mice.

A 5-year-old girl has lipoid proteinosis, causing voice issues, hair thinning, skin lesions, and tongue movement problems.

Personalized treatment based on detailed tumor analysis successfully managed and reduced the patient's aggressive hair follicle cancer.

A 19-year-old male had two rare skin conditions causing scarring and permanent hair loss.

A new treatment using unactivated platelet leukocyte autoplasma cured 80% of non-scarring alopecia patients.

Keratin is crucial for skin barrier formation and affects mitochondrial function.

Syphilis treatment resolved hair loss and eye symptoms, highlighting its importance in diagnosing unusual alopecia.

Genetic changes in specific proteins contribute to hair loss in some women of African descent.

6.1% of patients seeking PRP for hair loss had undiagnosed cicatricial alopecia, which PRP cannot treat.

Mutations in the hairless gene cause a rare form of permanent hair loss.

Keratin 19 may help diagnose and treat certain types of permanent hair loss.

A new gene location for Keratosis follicularis squamosa was found on chromosome 7p14.3-7p12.1.

Neural crest-derived progenitor cells in the cornea could help treat corneal issues without transplants.