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A different gene near the hairless gene on chromosome 8p21 causes a rare hair loss condition in a German family.

Testosterone therapy seems safe and effective for transgender men with proper care, but more long-term research is needed.

To stop online sexism, both men and women need to change how they act.

Higher fluoride levels may delay puberty in boys.

The photolyase-based device significantly changed the size and heat of potential skin cancer areas in patients.

Lichen Planopilaris in teens is rare, often misdiagnosed, and responds well to steroids.

The monkey's hair loss was due to an autoimmune disease, not genetics.

Photodynamic therapy was effective in treating multiple scalp basal cell carcinomas with minimal side effects and good cosmetic results.

Researchers found a gene mutation responsible for a rare hair loss condition.

A woman with acromegaloidism and normal growth hormone levels had a rare X-Tetrasomy, suggesting a need to study X-chromosome genes for their role in growth and facial development.

Women with nonclassic congenital adrenal hyperplasia experience more sexual dysfunction and distress.

Young women with nonclassic congenital adrenal hyperplasia may experience worse sexual function and mild depression compared to healthy women.

A 10-year-old boy had the earliest reported case of hair that became progressively kinkier but eventually returned to normal on its own.

Some children with localized scleroderma are rarely resistant to methotrexate, and no common profile for resistance was found.

Simvastatin may help manage symptoms in women with non-classic congenital adrenal hyperplasia by lowering cholesterol and certain hormone levels.

Applying minoxidil can help improve hair growth in people with hair loss caused by LIPH gene mutations.

Certain gene variations might help protect against insulin resistance and glucose intolerance in people with Polycystic Ovary Syndrome.

The document concludes that early and personalized treatment for PCOS in adolescents is crucial to manage symptoms and prevent long-term health issues.

The document concludes that early diagnosis and a comprehensive treatment plan are crucial for managing hair loss in children, with a focus on both medical and psychological support.

A rare combination of halo nevi, nonsegmental vitiligo, and early gray hair can occur together.

Getting ethical approval for research with children is important but can be complex and time-consuming, sometimes leading to the exclusion of certain age groups.

The p.P25L mutation in the KRT5 gene causes a rare skin condition that worsens over time and may lead to hair loss starting in young adulthood.

Hair loss was found in 37.4% of surveyed rural high-school students in Eskisehir, Turkey, affecting their quality of life, especially in general health and mental well-being.

Late diagnosis of congenital adrenal hyperplasia can greatly affect physical development, gender identity, and sexual health.

Cinnamon bark extract may help prevent weight loss and hair loss in breast cancer patients during chemotherapy and is safe to use.

Some IBD patients on anti-TNFs developed severe skin issues, but ustekinumab helped.

Children with cancer had slightly more unusual facial shapes than healthy kids, but not enough to easily tell them apart.

Women with nonclassical congenital adrenal hyperplasia may have a higher risk of fertility issues and miscarriages, and should get genetic counseling.

A Saudi girl was diagnosed with Loose Anagen Hair Syndrome, a rare condition causing easy hair loss without scarring.

The robotic system for hair restoration surgery works well, giving similar results to manual techniques after 9 months.