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A new method was created to measure metformin in hair, showing potential for monitoring treatment and medical investigations.

Researchers found genetic mutations causing hypohidrotic ectodermal dysplasia in 88% of studied patients and identified new mutations and genetic variations affecting the disease.

Some congenital hair disorders improve in childhood or with treatments like minoxidil and retinoids, while others like Netherton syndrome and trichothiodystrophy have a poor prognosis.

Manganese levels in hair may be linked to multiple sclerosis.

Genetic variations contribute to over 10% of recurrent early pregnancy loss cases.

AMPK activation may reduce melanoma risk in red-haired individuals.

Myhre syndrome symptoms worsen over time, with specific genetic variants affecting severity.

Identical twins had different symptoms because one had more cells with an extra chromosome fragment in different tissues.

A three-year-old girl has hair loss despite treatment with selenium sulfide shampoo and anti-fungal medication.

The study found genetic diversity in coat color dilution among Czech pointers in Slovakia.

Mitochondrial dysfunction may contribute to chronic inflammation and immune system issues in Lichen planopilaris.

Premature graying of hair is mainly caused by genetics, stress, and environment, with potential treatments being explored.

Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.

Dermoscopy helped diagnose a rare hair disorder in a 2-year-old boy.

Monilethrix has no effective treatment, but avoiding hair trauma helps manage it.

Low selenium levels worsen health but increase lifespan in mice.

Different problems with hair stem cell renewal can lead to hair loss.

Polyamines help repair DNA breaks and may influence cancer development.

ODC1 gene mutations cause a neurodevelopmental disorder with large head size, hair loss, and facial abnormalities.

Valproate can cause hair problems, but there are ways to manage them.

Deleting the MAD2L1 gene is tolerated in certain mouse cancer models.

Insufficient androgen action in male fetuses can cause genital development issues due to genetic mutations or environmental chemicals.

Budesonide and N-acetylcysteine reduced tumors and alopecia in mice, regardless of FHIT gene status.

Most patients with rheumatoid arthritis continued methotrexate treatment over two years, but those who stopped and restarted experienced more side effects and less improvement.

H3K4me3 helps control RSPO3 to influence hair growth and development.

Trichoscopy can diagnose monilethrix, a genetic hair defect causing hair thinning and loss.

Maneb causes delayed hair follicle damage in rats.

Minoxidil helps restore thymus size in 22q11.2 deletion syndrome.

ME1 and PPAR signaling may influence hair loss in androgenetic alopecia.