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Blocking the prolactin receptor might help treat various diseases, but more research is needed.

EVG staining is a valuable, simple, and cost-effective method for diagnosing various skin conditions in dermatopathology.

Testosterone causes hair loss in AGA mice, which are good for testing baldness treatments, and both minoxidil and cyproterone acetate can prevent this hair loss.

Use minoxidil for hair loss treatment, and finasteride for men.

Hair loss requires customized treatments based on its various causes and types.

Hair follicle hyperplasia is common in both benign and malignant skin lymphoproliferative disorders, with a proposed new term "pseudolymphomatous adnexitis."

Finasteride treatment in male rats causes long-lasting effects on depression-like behavior, brain cell growth, inflammation, and gut bacteria composition.

The review found no clear link between vitamin D receptor gene variations and polycystic ovary syndrome.

Losing eyelashes or eyebrows can be a sign of many different health problems and needs a careful approach to treat effectively.

The document concludes that there is no clear definition of adequate health insurance, and a consistent method to measure underinsurance is needed.

Eating glucoraphanin can help prevent psychosis in offspring whose mothers had immune system activation.

DHT's role in hair loss is important, but measuring its level for diagnosis is questionable.

Prostaglandin E2 affects human platelet activity in complex ways that could lead to personalized heart disease treatments.

Potassium channel openers like minoxidil help hair grow by acting on hair follicles.

Hair loss common in Norwegian men, affecting self-esteem and life quality.

Some treatments work for common baldness, but there's less evidence for other hair loss types, and more research is needed.

Existing drug dexamethasone may lower death risk in severe COVID-19 cases; more research needed for other drugs.

Type I interferons play a key role in the development of various skin diseases.

Dutasteride makes alcohol less sedating and may lead to less drinking in men.

The document concludes that inherited epidermolysis bullosa is a challenging genetic condition requiring multidisciplinary care and new treatments.

FOXN1 gene mutations cause a rare, severe immune disease treatable with cell or tissue transplants.

The document describes a woman with familial Parkinson's disease due to a genetic mutation, showing severe symptoms and poor response to treatment, and suggests finasteride may help reduce symptoms in Tourette syndrome.

Patient-derived melanocytes can potentially treat vitiligo by restoring skin pigmentation.

Low testosterone and 5α-reductase inhibitors can harm men's metabolic and sexual health; testosterone therapy may help, but discussing 5α-RIs' side effects is important.

Oral retinoids are effective for treating severe skin disorders but have reversible side effects and risks for pregnant women.

Patients with Alopecia areata have fewer specific immune cells that normally regulate the immune system, which may contribute to the condition.

Certain HSD3B1 gene types are linked to worse prostate cancer outcomes and affect treatment response and other health conditions.

The document concludes that managing non-classical congenital adrenal hyperplasia in females requires personalized treatment, genetic counseling, and a team of specialists.

Diagnosing PCOS in teenagers is hard because its symptoms often look like normal puberty, and there's a need for better diagnosis methods and agreement on criteria.

Nonclassic congenital adrenal hyperplasia is a genetic disorder causing hormone imbalances, affecting fertility and requiring personalized treatment.