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Two new compounds were found to build bone and muscle without affecting reproductive organs and skin oil glands.

There are various effective hormone treatments for puberty induction in boys and girls with hypogonadism, and starting treatment early is important.

Taking tadalafil and finasteride together is safe and effective for treating urinary symptoms and erectile dysfunction in men with enlarged prostates.

About 50% of 46, XY DSD cases lack a genetic diagnosis, but advanced sequencing methods improve detection.

The link between anabolic agents and colorectal cancer risk is unclear.

Early detection of specific VDR mutations is crucial for effective treatment and better dental outcomes in children with hereditary vitamin D–resistant rickets.

Three new gene mutations cause rickets and hair loss, treatable with high calcium and calcidol, but hair regrowth is rare.

Mice without the enzyme HSD17B3 still produce normal testosterone, suggesting they have different ways to make it compared to humans.

The testes produce sperm and hormones essential for male development.

Lung and liver macrophages protect our tissues and their dysfunction can cause various diseases.

New SRD5A2 variants may disrupt protein function, aiding diagnosis and treatment of related disorders.

Dermatologists are crucial in providing personalized care for patients with sex development differences.

Zinc is crucial for health, and deficiency can lead to immune, digestive, skin, and metabolic issues.

Hypochlorous acid is a safe, effective antimicrobial with potential in various medical fields, but more research is needed to improve its stability and use.

Accurate diagnosis and early specialist referral are crucial for managing 46,XY Disorders of Sex Development.

Melatonin promotes hair growth and quality by enhancing hair follicle development and reducing stress.

A 15-year-old girl with no menstrual period was diagnosed with a genetic condition that makes her body unable to respond to male hormones, leading to female characteristics despite having male genetic makeup.

Patients with Complete Androgen Insensitivity Syndrome need psychological support and multidisciplinary care for complex treatment decisions.

Three siblings with a rare genetic condition had abnormal sexual development and chose different gender identities, needing surgery and therapy.

Lichen planus is not linked to metabolic syndrome, but it is associated with higher rates of high blood pressure, high triglycerides, and low HDL cholesterol.

Men with male pattern baldness don't necessarily have high levels of Dehydroepyandrosterone-sulfate, and there's no link between its levels and the severity of hair loss.

Targeting the Smoothened receptor shows promise for treating certain cancers.

Houttuynia cordata compounds may help with anti-aging and hair loss.

Testosterone replacement therapy should be used for men with low testosterone levels and symptoms of hypogonadism, after careful diagnosis and considering individual needs.

Stabilizing HIF-1A in hair follicles may reduce oxidative stress and promote hair growth by increasing glycolysis.

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A new mutation in the HR gene is linked to a rare form of hair loss with limb deformities.

CTHRC1 helps hair grow back, and plantar dermis mixture boosts it.

Researchers found key regions in the mouse hairless gene that control its activity in skin and brain cells, affecting hair follicle function.