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PDRN may reduce inflammation and complications in revision rhinoplasty for patients with high fibrinogen levels.

Aging in one type of stem cell can cause aging-like changes in various organs.

Increased ODC expression makes normally tumor-resistant mice more prone to tumor development.

Neurosteroids may help treat disorders with too much dopamine activity.

New mutations in hair keratin genes can change hair structure and cause monilethrix, with nail issues more common in certain gene mutations.

Disrupting the FGF5 gene in rabbits leads to longer hair by extending the hair growth phase.

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

Serum AMH is a useful biomarker for diagnosing PCOS.

A new syndrome, Teelwani Syndrome, combines features of two rare genetic disorders.

Certain microRNAs in the fluid around eggs are linked to Polycystic Ovary Syndrome and may help diagnose it.

Hutchinson-Gilford Progeria Syndrome causes rapid aging from a genetic mutation, with no cure but ongoing research into potential treatments.

AMH and ovarian morphology help diagnose and understand PCOS more precisely.

The study found that certain microRNAs are higher in the cells and lower in the fluid of women with a specific type of polycystic ovary syndrome, and one microRNA could potentially help diagnose the condition.

Normal-range ALT levels can indicate metabolic and hormonal imbalances in young women.

Overexpressing Merkel cell virus proteins in human hair follicles can create clusters of cells that resemble Merkel cell cancer.

Blocking α1-integrin makes adult fibroblasts more like foetal ones, improving their movement and aiding wound healing.

Many lupus patients experience hair loss, which is linked to anxiety and other skin issues.

A new syndrome was linked to two new genetic changes in the MBTPS1 gene in a 14-year-old girl.

Two brothers from Bangladesh were diagnosed with X-linked adrenoleukodystrophy, showing neurological and adrenal symptoms.

Hutchinson-Gilford Progeria Syndrome causes rapid aging due to a gene mutation, with no cure yet, but research may lead to better treatments.

A woman with a specific mutation causing adrenal gland issues faced fertility problems, but careful hormone therapy helped her manage it successfully.

Facial skin aging is influenced by wrinkles, spots, genetics, and environment.

The SAM model helps understand aging and related diseases.

Keratin 17 is important for hair and nail structure and affects pachyonychia congenita symptoms.

K16 can partially replace K14 but causes hair loss and skin issues.

Higher thyroid hormone levels may be linked to certain types of polycystic ovary syndrome.

Early diagnosis and personalized treatment for PCOS are crucial, especially for young women in West Bengal, India.

A gene deletion in mice causes weak protein, immune issues, hair loss, airway problems, and wasting disease.

Different gene mutations cause different types of ichthyosis, with some new mutations found.