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Insulin resistance is linked to high male hormone levels in women, often seen in those with PCOS.

Baricitinib for severe alopecia areata is generally safe, with common side effects like infections and acne, and low rates of serious complications.

Family members of North Indian women with PCOS have a high rate of metabolic syndrome.

Hair loss in systemic lupus erythematosus patients is unique and improves with treatment.

Estrogens are key for bone growth spurts in both boys and girls and affect growth into adulthood.

The document concludes that combination therapy is most effective for treating excessive hair growth in women with idiopathic hirsutism, and more research is needed to understand the condition.

Environmental factors like diet and vitamin levels, especially Vitamin D, can affect autoimmune diseases differently, with lifestyle changes potentially improving outcomes.

The document concludes that hair follicles have a complex environment and our understanding of it is growing, but there are limitations when applying animal study findings to humans.

A new mutation in the TMEM173 gene and a risk allele in IFIH1 cause a unique set of immune-related symptoms.

Looking older on the outside might be linked to aging faster on the inside and can be affected by lifestyle choices and health risks.

Skin symptoms can indicate endocrine disorders and have various treatments.

The document summarizes medical findings on topics like heart rhythm treatment, sleep apnea therapy, and various health conditions and treatments.

Cetaceans lost hair due to changes in the Hr and FGF5 genes.

Female pattern hair loss is common and should be treated early to prevent worsening, with Minoxidil being the main approved treatment.

Hair follicle stem cells are key for hair and skin regeneration, can be reprogrammed, and have potential therapeutic uses, but also carry a risk of cancer.

In vivo reflectance confocal microscopy is useful for evaluating hair shaft diseases but needs improvement for deeper hair follicle issues.

The methylation of the HOXC8 gene's exon 1 affects cashmere fiber length in goats.

Sheep and goat hair fibers are complex due to keratin-associated proteins, which are important for fiber properties and growth.

Early diagnosis of Trichorhinophalangeal syndrome type 1 is crucial for treatment and was achieved through clinical examination and family history.

A new mutation in the CDH3 gene causes hair loss and vision problems in a young girl.

The KRTAP21-1 gene affects wool yield and can help improve wool production.

Alopecia areata in Taif is common, mainly immune-related, and best treated with topical corticosteroids and vitamins.

Understanding hair growth involves complex factors, and more research is needed to improve treatments for hair loss conditions.

The KRT84 gene is linked to better wool quality in Gansu Alpine Fine-wool sheep.

Understanding hair follicle development can help treat hair loss, skin regeneration, and certain skin cancers.

The document concludes that mouse models are helpful but have limitations for skin wound healing research, and suggests using larger animals and genetically modified mice for better human application.

Skin aging is a complex process influenced by various factors, leading to wrinkles and sagging, and should be considered a disease due to its health impacts.

Scarless healing is complex and influenced by genetics and environment, while better understanding could improve scar treatment.

The document concludes that mouse models are crucial for studying hair biology and that all mutant mice may have hair growth abnormalities that require detailed analysis to identify.

G allele of AR Stul polymorphism linked to higher hair loss risk, especially in white people.