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New therapies for Birt–Hogg–Dubé syndrome are being developed based on understanding the FLCN gene's role.

Keratin proteins are essential for keeping the cells in the human colon healthy and stable.

Adults should not consume more than 255 micrograms of selenium per day to avoid risk of hair loss and other side effects.

Genetic discoveries are leading to new treatments for alopecia areata.

Testosterone can help premenopausal and postmenopausal women with low sexual desire, but its long-term safety is unclear and it's not widely approved for this use.

Some steroid-induced health issues in rodents improved after stopping treatment, but hair loss and eye problems did not.

Lipocalin-Type Prostaglandin D2 Synthase (L-PGDS) is a protein that plays many roles in the body, including sleep regulation, pain management, food intake, and protection against harmful substances. It also affects fat metabolism, glucose intolerance, cell maturation, and is involved in various diseases like diabetes, cancer, and arthritis. It can influence sex organ development and embryonic cell differentiation, and its levels can be used as a diagnostic marker for certain conditions.

Finasteride and dutasteride are equally effective and safe for treating benign prostatic hyperplasia.

Cronkhite-Canada syndrome is a rare, non-inherited condition causing various symptoms like polyps, hair loss, and weight loss.

Genetic defects in the glucocorticoid receptor gene can cause conditions with abnormal sensitivity to stress hormones, and other factors may also affect this sensitivity.

Growth hormone levels affect hair growth and loss, with too much causing excess hair and too little leading to hair loss.

Spironolactone does not increase cancer risk and may lower prostate cancer risk, but more research is needed.

Eating too much selenium can cause bad breath, hair loss, and nail changes, with harmful effects starting at low daily doses.

More high-quality research is needed to recommend flavonoids and saponins for clinical use.

Cronkhite-Canada syndrome may be more treatable and less severe than previously thought.

High androgen levels in postmenopausal women may suggest an ovarian tumor, and removing it can improve heart and metabolic health.

Women experience more side effects and have worse blood pressure control from hypertension treatments than men, despite using different medications.

GnRH analogue can help diagnose ovarian causes of high testosterone in postmenopausal women when scans don't show the cause.

ATP-sensitive K+ channel subunits, particularly Sur2A, play a significant role in various cancers.

Nanocarriers can improve the effectiveness of herbal medicines in treating colorectal cancer.

Albumin and prednisone improved symptoms in a woman with Cronkhite-Canada syndrome, revealing potential genetic causes.

Eruptive vellus hair cysts are often missed in diagnoses.

A diabetic cat with another gland issue got better after treatment with cabergoline, no longer needing insulin.

Testosterone is key for male sexual function, and treating hormone imbalances can improve sexual issues.

Regular endoscopic checks are crucial for Cronkhite-Canada syndrome patients to catch potential cancers early.

Endocrine diseases in children often cause skin changes like dryness, redness, acne, hair loss, and more.

Preventing cancer involves lifestyle changes, vaccinations, early screening, and understanding cancer's molecular basis.

Nanoformulations improve luteolin's effectiveness as a cancer treatment.

Cronkhite-Canada syndrome is rare, has a poor prognosis, and requires early diagnosis and ongoing treatment.

Ovarian hyperthecosis should be considered in young women with severe male-like symptoms and can be managed with hormone treatments.