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5-alpha reductase inhibitors, like finasteride and dutasteride, are used for prostate issues, hair loss, and excessive hair growth, may help with COVID-19, but can cause sexual and mental health side effects, and their use in preventing prostate cancer needs more examination.

5-alpha-reductase inhibitors can lower prostate cancer risk but may increase high-grade tumors and cause sexual side effects.

5 alpha-reductase inhibitors like finasteride may lower prostate cancer risk and improve cancer screening.

Puerariae Flos extract may help treat hair loss by blocking a hair loss-related enzyme and promoting hair growth.

The human type II 5α-reductase gene, linked to certain male health conditions, has a specific structure and low similarity to other related genes.

The human type II 5α-reductase gene has a specific structure important for understanding certain medical conditions.

Some newly made compounds are promising for treating enlarged prostate, hair loss, viruses, and prostate cancer, and might be better than current drugs.

Medications for enlarged prostate can cause sexual side effects like reduced libido, erectile dysfunction, and ejaculatory problems.

Dutasteride use can lead to a stable decline in sexual function that is not affected by age or prostate size.

Three compounds were found to inhibit a prostate disease-related enzyme and reduce prostate size more effectively than the current treatment, suggesting they could be used for treating benign prostatic hyperplasia.

Finasteride safely treats enlarged prostate and male-pattern baldness.

Melandrium firmum extract helps mice grow hair by blocking a hair loss enzyme and changing hair growth genes.

Taking both finasteride and dutasteride for prostate issues may raise the risk of heart problems.

Dutasteride is more effective than Finasteride in reducing prostate size and PSA levels, but both drugs have similar side effects.

α-Blockers and 5-ARIs for BPH can cause sexual dysfunction, including erectile and ejaculatory issues.

The substance MK386 effectively blocked testosterone conversion and reduced cell growth in certain skin cells, but inhibiting 5α-reductase alone may not greatly improve acne.

Steroids, particularly estrogens and 5α-reductase inhibitors, affect blood vessel-related hair growth processes in hair follicle cells.

Frontal Fibrosing Alopecia's cause is unclear, affects mainly postmenopausal women, and current treatments focus on stopping hair loss rather than regrowth.

Post-finasteride Syndrome causes lasting negative effects, but more research is needed for treatment and risk evaluation.

The new progesterone derivatives effectively inhibit 5α-reductase and bind to the androgen receptor.

Some medications may cause lasting sexual dysfunction.

Finasteride improved symptoms in a schizophrenia patient.

Personalized treatment with inhibitors, minoxidil, and laser therapy helps hair loss.

Hair loss in Androgenetic Alopecia is caused by genetics, aging, and lifestyle, leading to hair follicle shrinkage and related health risks.

Finasteride and Dutasteride can improve hair growth in male baldness but may cause temporary sexual dysfunction and possibly affect fertility.

New pregnane derivatives were more effective than finasteride at inhibiting a key enzyme for male pattern baldness.

Low androgen levels might delay prostate cancer but could lead to more aggressive, therapy-resistant cancers.

The study found that the average age of women diagnosed with Frontal Fibrosing Alopecia in Argentina is higher than in other countries, but their symptoms are similar.

Heredity and hormones cause common hair loss, and topical minoxidil is the first recommended treatment.

Hormonal therapies help treat female hair loss, but results are slow and vary.