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Finasteride reduces hair growth better, but spironolactone has more side effects.

Hidradenitis suppurativa treatment should be tailored to the individual, with quitting smoking being important.

The document concludes that understanding hair and feather regeneration can help develop new regenerative medicine strategies.

There are still challenges in diagnosing and treating chronic skin diseases, but there is hope for future improvements.

5α-reductase inhibitors increase the risk of sexual dysfunction, especially in men with enlarged prostate.

Androgens play a complex role in skin conditions like acne and hair loss in women, and normal blood levels don't always show true androgen status.

Research on epidermal stem cells has advanced significantly, showing promise for improved clinical therapies.

FOXN1 gene variants cause low T cells and immune issues from birth.

Different harmful mutations in the CDH3 gene cause HJMD, but symptoms vary among individuals.

Oral retinoids are effective for severe skin conditions but require careful use due to side effects.

The document concludes that more research is needed to understand excessive hair growth in women with normal hormone levels and regular ovulation.

Researchers established normal hair and scalp characteristics for healthy women using trichoscopy.

Male genital development is driven by androgen signaling and understanding it could help address congenital anomalies.

A gene variant in KRT71 causes the curly fur in Selkirk Rex cats.

Hair follicle hyperplasia is common in both benign and malignant skin lymphoproliferative disorders, with a proposed new term "pseudolymphomatous adnexitis."

FOXN1 gene mutations cause a rare, severe immune disease treatable with cell or tissue transplants.

The document concludes that early diagnosis and treatment are crucial for children with hair loss to prevent permanent damage, although not all conditions can be effectively treated.

Hair disorders are caused by a complex mix of biology, genetics, hormones, and environmental factors, affecting hair growth and leading to conditions like alopecia.

Wnt/ß-catenin signaling is crucial for regulating skin stem cells and hair growth, with the right levels and timing needed for proper function.

Different populations have distinct hair structures related to their ancestry.

Gene therapy, especially using atoh1, shows promise for creating functional sensory hair cells in the inner ear, but dosing and side effects need to be managed for clinical application.

ESR2 gene variations may be linked to female pattern hair loss.

The study found no common cause for a girl's crystalline cataract and uncombable hair, suggesting their co-occurrence might be coincidental.

African American men with prostate cancer have more androgen receptor mutations, which may lead to more aggressive cancer compared to Caucasian American men.

Epidermal stem cells have various roles in skin beyond just maintenance, including forming specialized structures and aiding in skin repair and regeneration.

A 2-year-old boy with a rare brain malformation may have Gomez–López-Hernández syndrome.

Male pattern baldness may be caused by scalp pressure on hair follicles, which increases with age and leads to a cycle of hair loss. This process is not directly determined by genes.

P-cadherin is important for hair growth and health, and its problems can cause hair and skin disorders.

Finasteride side effects in young men may be linked to specific gene variations.

The transition from growth to regression in Cashmere goat hair follicles involves changes in expression of genes related to keratin and cell differentiation.