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Faulty inflammasome activation may lead to autoimmune skin diseases and could be a target for new treatments.

Hairless mammals have genetic changes in both their protein-coding and regulatory sequences related to hair.

Low serum ferritin levels are not closely linked to telogen effluvium in women.

The document concludes that better tools are needed to measure skin disease severity in dermatomyositis and cutaneous lupus erythematosus, and introduces the DSSI and CLASI as reliable instruments.

Molecular diagnostics help identify genetic defects causing endocrine diseases, improving diagnosis and treatment options.

Alopecia areata treatment should be personalized, using topical or systemic therapies based on severity, with promising options like JAK inhibitors needing more research.

Immune cells are crucial for hair growth and preventing hair loss.

Severe alopecia areata greatly impacts quality of life, mental health, and daily activities.

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

The document concludes that non-endocrine alopecia in pets varies in treatment effectiveness and often has a poor prognosis, especially in cats.

The Polish Dermatological Society recommends personalized treatment for cutaneous lupus, including lifestyle changes, medications, and monitoring, with specific drugs for severe cases.

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.

Cosmetic procedures can harm hair, but damage can be minimized with knowledge and care; however, once hair is damaged, it cannot be reliably repaired.

Benign skin tumors need accurate diagnosis to ensure proper treatment.

Genetic mutations can affect female sexual development, requiring personalized medical care.

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

Any medication can cause skin reactions, some due to allergies and others due to dosage or genetic factors.

Natural products like propolis are causing more skin allergies, and certain skin treatments and medications have various side effects and risks.

Eating more protein during weight loss can prevent hair loss caused by not having enough protein.

Penicillamine can cause taste problems due to copper loss, which can be fixed with copper or zinc supplements.

Endoscopic forehead and brow lifting safely and consistently improves aged eyebrows, but may have complications.

Recombinant thrombomodulin can effectively treat severe complications in Cronkhite-Canada syndrome.

Certain genetic changes in the LSS gene cause a rare skin and hair condition.

Hair loss in children is often caused by scalp infections, immune disorders, hair pulling, stress, and requires careful treatment due to emotional effects.

Primary cicatricial alopecia, a rare disorder causing permanent hair loss, is hard to diagnose and treat, with treatments like anti-inflammatory drugs and steroids offering varied results and no guaranteed cure. Psychological support for patients is important, and future research should aim to identify causes of the condition.

Mutations in specific keratin genes cause improper hair structure in mice due to faulty keratin protein assembly.

Older mice have stiffer skin with less elasticity due to changes in collagen and skin structure, affecting aging and hair loss.

Trichotillomania treatment is most successful with a mix of behavioral therapy, medication, and social support.

Marine microbes could be used in cosmetics for sun protection, skin care, and possibly preventing hair loss.