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Older adults commonly experience hair loss and nail disorders due to aging and health changes, affecting their quality of life.

A specific gene mutation causes varying hair loss severity in a Pakistani family.

Contact allergies might contribute to frontal fibrosing alopecia.

Thyroid diseases may contribute to autoimmune skin diseases, and more research is needed on their relationship.

The document concludes that understanding how adult stem and progenitor cells move is crucial for tissue repair and developing cell therapies.

Balding people may have higher heart disease risk.

The document concludes that ongoing research using animal models is crucial for better understanding and treating Alopecia Areata.

Rosemary's antioxidant content changes with the climate and season.

Boreal caribou in northeastern British Columbia have significant health issues, including infections, tick infestations, and mineral deficiencies.

Keratosis pilaris is often linked to genetic mutations and causes skin and hair abnormalities, regardless of those mutations.

Genes affect cytokine production, which can influence chronic diseases, and certain interventions may help prevent related molecular damage.

High hair cortisol levels indicate stress in cows due to poor shelter conditions and health issues.

Nellore cattle have genetic variations linked to their adaptation to tropical environments.

Various potential triggers may be causing the rise in frontal fibrosing alopecia, and avoiding these could help stop the disease's increase.

Hair gets thinner, grayer, and changes texture with age due to genetics, environment, and cellular changes, affecting the growth cycle.

Smoking and drinking worsened hair loss in men with genetic hair loss, while eating and sleeping habits didn't; genetics played a bigger role than environment in hair loss.

Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.

Ultraviolet rays damage hair, smoking may cause hair loss, and good nutrition is important for hair health, but genetics mainly decide hair thickness.

Children's hairlines change shape as they grow, with women often developing a widow's peak and men's hairlines becoming more convex and possibly balding at the temples, influenced by genetics and hormones.

Non-Kuwaiti COVID-19 patients had worse health outcomes than Kuwaitis, likely due to poorer socioeconomic conditions.

A new mutation in the PLEC gene causes a rare condition with skin blistering, muscle weakness, and hair loss.

Healthcare organizations must seriously focus on strategic decision-making to succeed in a complex market.

The 3D structure of a key hair protein was modeled, revealing specific helical structures and stabilization features.

The hair of two ancient Chilean mummies is well-preserved and contains high levels of heavy metals.

The document concludes that Follicular Unit Extraction is an advanced, less invasive hair transplant method with fewer side effects than traditional methods.

Indian dermatosurgical practitioners were given guidelines in 2011 to reduce infection risks, including hand hygiene, sterilization methods, operation theater standards, and proper waste disposal.

FPHL is common in women, influenced by genetics and hormones, and can be treated with medications, laser therapy, or hair transplantation.

Polycystic Ovary Syndrome (PCOS) in teenagers is a complex condition linked to genetics and environment, often associated with obesity and insulin resistance, and is treated with lifestyle changes and medication.

Polycystic ovary syndrome is a common hormonal disorder in women, linked to increased risk of metabolic and heart diseases, and needs more research for better understanding and treatment.

Men with more vanadium in their blood and who drink less soy milk are more likely to have hair loss.