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Certain genetic variations in the SHBG gene are linked to an increased or decreased risk of PCOS in Mediterranean women.

People with pattern hair loss have higher polyamine levels in the top of their head compared to the back.

Netherton's syndrome may have a familial link and doesn't always include atopy.

A new genetic model may improve treatment and diagnosis for certain inherited skin diseases.

A genetic change in the EDAR gene causes the unique hair traits found in East Asians.

Mice with a Gsdma3 gene mutation have thicker skin and longer hair follicle openings due to increased β-catenin levels.

DNA analysis can help tailor alopecia treatment.

Researchers identified genes in scalp hair follicles that may affect hair traits and hair loss.

DNA virus-induced tumors have consistent isozyme profiles, unlike other tumor types.

Progesterone and its metabolites affect myelin protein expression differently in male and female rat Schwann cells.

Adults with Tatton-Brown-Rahman syndrome may have serious heart problems and need lifelong heart monitoring.

Certain gene variations might help protect against insulin resistance and glucose intolerance in people with Polycystic Ovary Syndrome.

Astrotactin proteins are important for brain and skin development and are linked to several neurodevelopmental disorders.

Antiviral medication valganciclovir may improve skin and hair in Trichodysplasia Spinulosa patients.

Most children with a common hemochromatosis genotype had elevated iron levels but no severe symptoms.

The document concludes that the human keratin gene cluster is complex, with a need for updated naming to reflect over 50 functional genes important for hair and skin biology.

A specific thyroid hormone resistance mutation may be linked to different types of hair loss.

A young Russian girl with Meier-Gorlin syndrome has two new mutations in the CDC6 gene.

Researchers found a genetic link for hereditary hair loss but need more analysis to identify the exact gene.

Mutations in the KRT16 gene can cause skin and nail disorders.

Men have more tryptophan in their hair than women, and it increases with age and is higher in darker and grey or white hair.

Mutations in the DSG4 gene cause specific hair and scalp issues.

Different keratins have unique expression patterns in mouse skin cells.

The mutant HR bmh protein mis-localizes in cells, affecting skin and hair development.

A specific gene mutation causes hair loss and potential eye issues, even if vision seems normal.

A gene deletion in DSG4 causes sparse hair in some Pakistani families.

Polygenic Score can help predict severe psoriasis and psoriatic arthritis.

A new type of hereditary hair loss in a Chinese family is linked to chromosome 2p25.1–2p23.2.

Combining genetic and physical trait analysis improves diagnosis accuracy for monogenic diabetes.