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Two new reliable Arabic questionnaires for measuring quality of life in women with PCOS were created, one for married and one for unmarried women.

The document concludes that more research is needed to reduce frequent hospital visits, addiction medicine education improves with specific training, early breast cancer surgery findings are emerging, nipple smears are not very accurate, surgery for older melanoma patients doesn't extend life, a genetic condition in infants can often be treated with one drug, doctors are inconsistent with blood clot medication, a certain gene may protect against cell damage, muscle gene overexpression affects many other genes, and some mitochondrial genes are less active in mice with tumors.

Mitochondrial dysfunction is linked to various skin conditions and could be a target for treatments.

Alopecia Areata affects people of all ages worldwide, is likely caused by genetic and environmental factors, and can lead to stress and depression, highlighting the need for treatments that address both physical and mental health.

Gender-affirming dermatology treatments generally improve mental well-being for transgender individuals, but more research is needed.

Inhibiting AP-1 changes skin tumor types and affects tumor cell identity.

Inhibiting AP-1 changes skin tumor types and affects tumor cell identity.

A Brazilian male with IFAP syndrome has a unique genetic variant causing his condition.

New treatments for alopecia areata show promise, but standardized guidelines are needed.

Women with nonclassic congenital adrenal hyperplasia experience more sexual dysfunction and distress.

Early diagnosis of Trichorhinophalangeal syndrome type 1 is crucial for treatment and was achieved through clinical examination and family history.

The 2023 guideline advises a detailed approach for PCOS, focusing on early detection, lifestyle and medical treatments, and managing health risks.

DNA changes in tetraploid wheat improve root growth and nitrogen use.

A new HRAS gene variant may cause a range of symptoms including intellectual disability and psychiatric issues.

Reduced Stx17 expression may contribute to Alopecia Areata.

Some children in Malaysia with symptoms have either profound or partial biotinidase deficiency, and early testing and treatment are important.

Genetic differences between young and old Tan sheep explain why their fleece changes from curly to straight as they age.

Four new cases of Bachmann-Bupp syndrome suggest potential for targeted treatment.

Targeted anticancer therapies can cause severe side effects similar to traditional chemotherapy, but with different types.

Mutations in the vitamin D receptor cause hereditary vitamin D-resistant rickets, leading to poor bone health and requiring high calcium doses for treatment.

A genetic mutation caused severe rickets and alopecia in an Indian patient, but high-dose calcium and phosphate treatment improved their condition.

A 20-year-old woman with a rare form of Turner syndrome showed improvement with hormonal therapy and needs comprehensive care.

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

CGF therapy may effectively treat psoriasis by reducing inflammation.

Cantú syndrome is caused by mutations in the ABCC9 gene.

A woman with a unique syndrome similar to TRPS has a genetic change near the TRPS1 gene, affecting its regulation.

Msx and Dlx genes are crucial for development, controlling cell behaviors like growth and differentiation through their roles as gene regulators.

Cells from certain embryo parts can induce head formation in another embryo, involving complex signaling pathways.

The new technique PÂTÉ improved the amount of scalp tissue removed in surgeries.

Pangolins have lost some skin-related genes, but kept others, leading to their unique scales and skin features.