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Newly found stem cells in horse hooves show promise for treating a hoof disease called laminitis.

Including special area involvement helps identify more psoriasis patients who may need systemic treatment.

A 4-year-old girl had a rare hair disorder affecting only part of her scalp.

Hutchinson-Gilford Progeria Syndrome causes rapid aging due to a gene mutation, with no cure yet, but research may lead to better treatments.

Early and aggressive treatment with individualized care plans is crucial for managing pediatric systemic lupus erythematosus.

A reliable method was developed to measure perospirone levels in human plasma for clinical use.

Human fetal placental stromal cell injections speed up healing and improve skin and hair recovery after radiation damage.

A woman's psoriasis improved after hepatitis C treatment with interferon, despite interferon's risk of worsening skin conditions.

PRC2 is not essential for hair follicle stem cell maintenance or hair growth.

Hidradenitis Suppurativa has genetic links, with certain gene mutations more common in patients and a third of cases having a family history.

Spironolactone helped reduce excessive facial hair in a woman with porphyria cutanea tarda.

Heat shock protein 27 is more present in the active growth phase of human scalp hair follicles.

A gene mutation worsens skin irritation in mice due to a lack of certain fats.

S100A6 is important for cell functions and can help diagnose and treat diseases.

Proactive physical therapy improved mobility, reduced fatigue, and pain in lupus patients.

The VSCAPSI is a helpful method for evaluating the severity of scalp psoriasis.

Polycystic ovary syndrome is found in 6.5% of unselected Caucasian women in Spain.

RSPO1 mutations in certain patients lead to skin cells that don't develop properly and are more likely to become invasive, increasing the risk of skin cancer.

Human dermal stem/progenitor cells can divide and differentiate more than hair follicle dermal papilla cells.

Samcyprone ointment is effective for treating common warts if a sensitization reaction occurs first.

Early recognition and a team approach are crucial for managing diffuse alveolar hemorrhage in antiphospholipid syndrome.

A new mutation in the ST14 gene broadens the understanding of ichthyosis-hypotrichosis syndrome.

A new one-step test can quickly identify skin cancer during surgery.

Allergic reactions to blood thinners are rare but can be serious, requiring careful management and alternative treatments.

A CCS patient with severe complications was successfully treated using combined therapies.

A reliable method was developed to detect hair growth compounds in products, ensuring safety and compliance.

Saw palmetto supplements may reduce prostate cancer cell growth without being toxic.

Spironolactone helps reduce fluid in the eye in Central Serous Chorioretinopathy, but doesn't improve vision and recurrence is common.

A new gene mutation caused a man's rare skin condition, Schöpf-Schulz-Passarge syndrome.

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