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Hormones like androgens, estrogen, thyroid hormones, and stress hormones can contribute to hair loss, and treatments target these hormonal imbalances.

Proretinal nanoparticles are a safe and effective way to deliver retinal to the skin.

Yellow dots and short vellus hairs are key signs for diagnosing alopecia areata using trichoscopy.

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

White piedra, a rare fungal infection, was diagnosed in two women in a northern climate.

Finasteride effectively treats enlarged prostate and male baldness, improves symptoms of hirsutism in women, but doesn't work for acne, and may delay prostate cancer progression with few side effects.

Dermoscopy is becoming essential for diagnosing skin conditions and is expected to be a standard tool for dermatologists.

The document concludes that PCOS in adolescents is complex and requires comprehensive care to manage its symptoms and associated health risks.

The study concluded that immune cells attacking hair follicles cause hair loss in alopecia, with genetics and environment also playing a role, and highlighted the potential of certain treatments.

Canine hair follicles have stem cells similar to human hair follicles, useful for studying hair disorders.

Eyelash alopecia areata often goes undiagnosed and can lead to complete eyelash regrowth, especially in younger patients.

The document discusses male and female pattern hair loss, its diagnosis methods, FDA-approved treatments like finasteride and minoxidil, their side effects, and the role of lifestyle changes.

The document concludes that it's important to recognize and treat hair loss in women of color, considering their unique hair characteristics and psychological impact.

FUE is a versatile hair transplant technique with many uses and good outcomes when performed with skill.

Regenerative medicine shows promise for improving hair and skin but needs more research for standard use.

Trichoscopy is a quick, accurate, and non-invasive method to diagnose and treat non-scarring hair loss.

The study mapped yak skin cells to understand hair growth better.

Scaffold-based strategies show promise for regenerating hair follicles and teeth but need more research for clinical use.

Alopecia areata is a chronic condition causing hair loss, with new treatments targeting the immune system showing promise.

Dandruff might be caused by changes in how hair follicles naturally release oils and an immune response to this imbalance.

People with hair loss conditions may also have thyroid disorders, but more research is needed to understand the connection.

Trichoscopy helps diagnose and manage different types of hair loss in the Indian population.

Low-dose oral minoxidil is safe for treating children's hair disorders.

Androgenetic alopecia is a common hair loss condition influenced by various factors and linked to psychosocial and cardiovascular issues.

The document concludes that understanding and managing hair loss in cancer patients is important, and more research is needed for better treatments.

Primary idiopathic pseudopelade of Brocq causes gradual, scarring hair loss with no effective treatment.

A calf in Scotland likely had Schmallenberg virus from its mother.

Cutaneous Lymphadenoma is a unique skin tumor with specific protein markers and common gene mutations that may cause continuous cell growth.

The document concludes that more research is needed to reduce frequent hospital visits, addiction medicine education improves with specific training, early breast cancer surgery findings are emerging, nipple smears are not very accurate, surgery for older melanoma patients doesn't extend life, a genetic condition in infants can often be treated with one drug, doctors are inconsistent with blood clot medication, a certain gene may protect against cell damage, muscle gene overexpression affects many other genes, and some mitochondrial genes are less active in mice with tumors.

A baby was diagnosed with IFAP syndrome due to a new genetic mutation, showing severe skin and developmental issues.