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Asian patients with Frontal Fibrosing Alopecia often lose eyebrow hair and respond well to combined antiandrogen or antimalarial and topical treatments.

A 12-year-old boy with a rare genetic condition has progressive hair loss with no effective treatment.

Non-classical 21 hydroxylase deficiency is an underdiagnosed cause of female hair loss and polycystic ovarian syndrome.

Men are increasingly interested in cosmetic treatments that enhance masculinity and address aging without downtime, with tailored approaches for different ethnicities and a focus on hair restoration and body contouring.

No significant link was found between the studied genes and female hair loss in the Polish population.

Human skin and hair color variation is mainly due to melanin produced by a few genes, with melanin protecting against sun damage.

Hirsutism is more linked to high androgen levels than acne or hair loss, and a mix of hormonal tests is best for diagnosis; certain treatments can reduce symptoms.

Caucasian and Asian women with PCOS generally show similar symptoms, except Asian women have less chest hair.

Most patients with frontal fibrosing alopecia had facial bumps, with Hispanic/Latino and premenopausal women being more affected, suggesting a more severe condition.

The book provides a guide to cosmetic surgery for people with darker skin, covering various treatments and addressing their unique skin characteristics.

The document concludes that managing PCOS effectively requires considering ethnic differences, obesity's impact, and ethical concerns in treatment approaches.

Elephantopus scaber has many health benefits, including antibacterial, antifungal, anticancer, and antioxidant properties.

Health care providers should address the emotional challenges of SLE patients with comprehensive care.

Acanthosis nigricans is a skin condition that may indicate a higher risk for insulin resistance and type 2 diabetes, and more research is needed to understand and treat it.

Dr. Samuel M. Lam's article concludes that skilled facial fat grafting can effectively restore facial volume and serve as a complement or alternative to traditional face-lifting methods.

Frontal fibrosing alopecia can affect African men and may be underdiagnosed.

Suriname uses many plants for beauty, with potential for a beauty industry, but more evidence is needed for product effectiveness.

A Jordanian family with Clouston syndrome has a common GJB6 gene mutation.

Men are more likely to get infectious skin diseases, while women are more prone to autoimmune and pigment-related skin conditions, influenced by biological and environmental factors.

The article concludes that surgeons should tailor facial surgery techniques for Asian males to their unique cultural and anatomical needs.

The review found that individualized treatment and teamwork are important for trichotillomania, and patients who followed through with treatment often improved.

Targeted therapies for lung cancer are effective but require careful management of side effects to benefit patients.

The document concludes that hirsutism is the main sign for diagnosing hyperandrogenism, which requires a detailed patient history and physical exam.

The pseudo 'fringe sign' can also appear in frontal fibrosing alopecia, not just in traction alopecia, showing that this condition may be more common than thought.

Black skin requires specific cosmetic practices, which can sometimes cause skin issues due to product misuse, and there's a need for better regulations in sub-Saharan Africa.

PCOS in lean women is a serious health condition with implications beyond fertility, affecting metabolism and increasing cardiovascular disease risk.

Skin problems in older people can indicate hormonal diseases, nutritional deficiencies, or conditions like diabetes, menopause, and HIV.

Early treatment with corticosteroids improved her eye condition significantly.

The document suggests treating individuals with nonclassic congenital adrenal hyperplasia who show symptoms, especially those related to excess male hormones.

Truncating mutations in the C2orf37 gene cause Woodhouse–Sakati syndrome.