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Sons of mothers with polycystic ovary syndrome (PCOS) have a higher risk of obesity and insulin resistance, possibly due to certain genes and factors passed down from their mothers.

Enzymes are classified into six types and are essential for many biological processes, with only a few targeted by drugs.

The study created a mouse model to better understand hair follicle stem cells' role in hair growth and repair.

Understanding the Y chromosome is key to male health, aging, and developing diagnostic tools.

New tools show that in fish, NPY increases feeding and somatostatin decreases it.

Targeting the Wnt/β-catenin pathway may lead to better treatments for hair loss.

Using existing drugs for new purposes could be a cost-effective way to treat chest pain and non-clogged heart arteries, with some drugs for lung blood pressure showing promise but needing more testing.

A new genetic mutation in the ODC1 gene causes developmental delay and other symptoms in a young girl.

Capivasertib improves survival in certain breast cancer cases but requires careful management of side effects.

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

A specific gene mutation is linked to a hereditary form of dystonia that responds well to certain medications.

Adults with classic congenital adrenal hyperplasia value medication that prevents weight gain from glucocorticoids the most.

Routine monitoring isn't needed for healthy patients on low-dose oral minoxidil, but is advised for those with kidney issues.

A new genetic disorder caused by an ODC1 mutation can be treated with DFMO.

Drug advertising has greatly increased, changing consumer behavior and raising concerns about its influence on healthcare and patient protection.

Finasteride can treat prostatic haematuria, but its use is controversial.

A specific ATR gene mutation is linked to a hereditary oropharyngeal cancer syndrome.

Adult spiny mice recover better from heart attacks than common lab mice.

Dermatologists need to know about cosmetics to help patients with skin issues and recommend safe products.

A specific gene mutation causes sparse, brittle hair in a family.

Altering the keratin 17 gene in mice hair follicles caused temporary hair issues, but changes were minimal and short-lived.

Different mutations in the 5 alpha-reductase-2 gene were found in affected individuals in the Dominican Republic, suggesting no common ancestry.

Two new gene mutations cause a rare hair disorder.

A new DSG4 gene mutation causes hair defects in a young girl.

Treatments for acute leukaemia lead to high remission rates, but relapses occur, requiring ongoing advancements in care.

Researchers found a new mutation in the EDA gene that likely causes missing teeth and mild skin symptoms in one family.

Vibration assisted analgesia reduces pain during corticosteroid therapy for alopecia.