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A woman with a rare autoimmune disorder had a blister on her eye and unique immune reaction, which was effectively treated with medication.

A truncated protein linked to breast cancer may change cell adhesion.

IL-2 treatment causes skin eruptions and other reversible side effects, and may play a role in psoriasis.

A 16-year-old boy's facial condition improved with doxycycline, suggesting an immune response to hair follicle damage.

A 61-year-old Filipino man had a skin condition that looked like another disease, making diagnosis difficult.

Certain genetic variants reduce enzyme activity, contributing to non-classic congenital adrenal hyperplasia.

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Certain genetic variants impair enzyme activity, contributing to non-classic congenital adrenal hyperplasia.

Dermatologists vary widely in testing practices for alopecia areata, often exceeding guideline recommendations.

The case suggests a possible autoimmune link between lichen sclerosus and vitiligo.

Removing certain hair follicle stem cells worsens skin reactions to allergens.

Leukemia can sometimes appear as unusual skin issues in children.

K31 can identify clear secretory cells in human sweat glands.

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

COVID-19 vaccination may trigger recurrence of cutaneous T-cell lymphoma in some patients.

Intralesional cidofovir may be a viable alternative treatment for SCC.

A woman with lymphoma had a rare skin rash on her scalp and forehead, which was hard to diagnose but responded well to treatment.

Interferon, especially alfa interferon, is an effective treatment for cutaneous T-cell lymphoma with manageable side effects.

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Most injecting drug users in the study had hepatitis C and skin problems, which moderately affected their quality of life.

Checkpoint inhibitor therapy can cause skin issues, from mild rashes to severe reactions.

High levels of ODC and a mutant Ha-ras gene cause tumors in mice.

High CRP levels could indicate vitamin D deficiency in people with alopecia areata.

Plasmacytoid dendritic cells, which overproduce IFN-α, may play a crucial role in starting alopecia areata, an autoimmune disease causing hair loss.

HSP90 and lamin A/C are crucial for hair growth and could be targets for treating hair loss.

A mutation in the hairless gene speeds up severe itchy skin in mice on a special diet.

Three specific mutations in the LIPH gene can cause hair loss by damaging the protein's structure and function.

Lymphoma should be considered in unusual scalp hair loss cases, as treatment can work but may lead to severe complications.