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Polycystic ovary syndrome, a disorder causing menstrual issues and infertility, can be treated with lifestyle changes, medication, herbal remedies, surgery, and assisted reproductive techniques like artificial insemination and IVF.

Androgen use may increase the risk of stroke, but more research is needed.

The protein STAT3 slows down cell growth by blocking the FST gene, which affects hair development in sheep.

The study found two new mutations in a Chinese patient with severe biotinidase deficiency.

A young woman with severe symptoms of CPAN improved with intensive treatment but needed a leg amputation.

Patients with alopecia areata may have lower vitamin D levels than healthy people.

A pet ferret had a serious infection from Mycobacterium xenopi, which can spread to humans.

Tadalafil and Finasteride may help treat aggressive melanoma.

Genetic screening for NUDT15 polymorphisms is crucial for patients taking azathioprine, especially in Asians.

Early recognition and treatment of SLE can improve outcomes in patients with complex symptoms.

High CRP levels could indicate vitamin D deficiency in people with alopecia areata.

UV exposure reduced hair shine in mice, but minoxidil helped restore it.

A 10-month-old boy with a rare combination of genetic conditions has severe immune deficiency and treatment challenges.

Neuropathic pruritus is a commonly overlooked and wrongly diagnosed type of chronic itching that is hard to treat.

A girl with a rare genetic disorder had a unique bone condition, highlighting the need for careful diagnosis and suggesting the disorder might be more common than thought.

Hair loss in women aged 20-30 is often linked to deficiencies in Vitamin D, zinc, ferritin, and haemoglobin, as well as low SHBG levels in those with irregular periods.

Some women with PCOS have rare genetic variants linked to the condition.

High levels of TNF-α may contribute to obesity and insulin resistance in PCOS, but not due to the C850T genetic variation.

EtG levels in hair decrease significantly after one month of alcohol abstinence.

KAP-depleted hair causes less immune response and is more biocompatible for implants.

The androgen receptor is a promising target for breast cancer treatment, especially in triple-negative cases, but more research is needed for personalized therapies.

Rapamycin may help treat Leigh syndrome by targeting protein kinase C.

The research reveals how early embryonic mouse skin develops from simple to complex structures, identifying various cell types and their roles in this process.

Adult esophageal cells can start to become like skin cells, with a key pathway influencing this change.

The unique coat of lykoi cats is likely caused by new variants in the Hairless gene.

Beta-caryophyllene, found in essential oils, helps wounds heal better in multiple ways.

Hairless mammals have genetic changes in both their protein-coding and regulatory sequences related to hair.

MendelVar is a tool that helps identify important genes by combining GWAS data with Mendelian disease information.

Certain cells in the adult mouse ear come from cranial neural crest cells, but muscle and hair cells do not.

Skin cell types develop when specific genes are turned on by removing certain chemical tags from DNA.