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Vitamin A deficiency changes cattle hair structure, while pregnancy may improve it, suggesting hair can indicate cattle health.

Early recognition and treatment of atypical alopecia areata in infants are crucial.

TNC+ fibroblasts play a key role in skin inflammation by interacting with T cells.

Certain gut bacteria may protect against alopecia areata, while others may increase the risk.

Most rural children with scalp ringworm had a non-inflammatory type and early treatment is important to prevent complications.

The hair tonic with cinnamon oil and coconut oil was stable and caused very mild irritation.

New research has found 14 genes linked to the risk of developing alopecia areata, improving understanding and treatment options.

The study aims to create a model to improve personalized and preventive health care.

Horse skin has a layered epidermis, a dermis with hair follicles, sweat and sebaceous glands, and is supplied by small arteries.

Testosterone and dihydrotestosterone treatments can help with penile growth in males with 5α-reductase type 2 deficiency, with dihydrotestosterone being more effective in infancy.

An 8-year-old girl has a rare genetic disorder causing complete, irreversible hair loss and skin bumps.

Nebivolol cream may be a promising hair loss treatment by improving blood flow and nourishing hair follicles.

People with Down syndrome have a higher risk of skin disorders and need better screening and treatment.

Researchers found a genetic link for hereditary hair loss but need more analysis to identify the exact gene.

Patients with RASopathies have a higher risk of autoimmune disorders and should be routinely screened.

Silk sericin dressing with collagen heals wounds faster and improves scar quality better than Bactigras.

Finasteride can have lasting negative effects on brain function and behavior by disrupting neurosteroid production.

The decision tree can predict drug absorption issues with good accuracy but needs more validation and adjustments for other factors.

The HoxC gene cluster and its enhancers are essential for developing hair and nails in mammals.

An 8-year-old girl has a rare, irreversible hair loss condition caused by a genetic mutation.

Understanding normal hair growth and loss in children is key to diagnosing and treating hair disorders.

People with pattern hair loss have higher polyamine levels in the top of their head compared to the back.

Targeted therapy with Ustekinumab significantly improved a skin condition called ILVEN, which is caused by mutations in the CARD14 gene.

Specialized ribosomes affect aging in human skin cells.

Researchers fixed gene mutations causing a skin disease in stem cells, which then improved skin grafts in mice.

The polyherbal emulgel created for hair care was safe, had good qualities, and could lead to future hair care products.

A gene variant causes patched hair loss in mice, similar to alopecia areata in humans.

Combining microneedling with platelet-rich plasma enhances skin repair and collagen production but may not offer significant extra benefits.

Different scalp and hair disorders are more common in certain ethnic groups, with the most common being androgenetic alopecia, which is treated with medications like minoxidil and finasteride.

Cancer rates are increasing in developed countries, with estrogen, aging, low vitamin D3, and HPV infection as common causes.