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A child has a rare hair and skin disorder due to specific gene variants, suggesting broader genetic testing is needed.

A new mutation in the STING protein causes a disease with lupus-like symptoms and responds well to a specific inhibitor treatment.

A keratin hHb6 mutation causes a hair disorder with varying severity, influenced by other factors.

Turning off the Lhx2 gene in mouse embryos leads to slower wound healing and scars.

A Chinese male with a new genetic mutation has a skin condition and severe urinary issues, with treatments having mixed success.

Two new mutations in the CDH3 gene cause hair loss and vision problems in a young girl.

A new mutation in the KRT86 gene was found to cause the hair disorder monilethrix in a Han family.

A boy had a rare scalp condition with thickened skin and different-colored hair.

A mutation in the HOXC13 gene causes hair and nail problems in a Syrian family.

A specific gene mutation causes congenital hair loss.

High lactate dehydrogenase activity is not necessary for the growth of squamous cell carcinoma.

A mutation in the MAP2 gene causes reduced hair follicle density, leading to hairlessness.

A 6-year-old Asian boy has a rare scalp condition causing hair loss and thickening, with unclear causes and no effective treatment.

The patient's hair was thinner and had fewer lipids due to a genetic mutation.

A new mutation in the CDH3 gene causes hair loss and vision problems in a young girl.

A gene mutation in mice causes permanent hair loss and skin issues.

A new genetic mutation was found causing hair and eye issues in a boy.

A mutation in the Sgkl gene causes defective hair growth in mice.

Lipedematous scalp may be underdiagnosed and doesn't improve with finasteride.

People with lichen planus are more likely to have abnormal blood fats than healthy people.

Higher activity in lichen planopilaris is linked to certain immune and tissue genes.

Scientists found gene mutations that affect hair loss, skin stem cells, and skin disorders, and identified drugs that may help treat blood vessel and skin conditions.

Mutations in the hHb6 gene cause the hair disorder monilethrix.

A new mutation in the Hairless gene causes hair loss in two Pakistani families.

People with lichen planus are more likely to have dyslipidemia, especially higher triglyceride levels.

FGF5 gene mutations cause long hair in domestic cats.

A Taiwanese patient had hair loss and skin bumps without the usual gene mutation, suggesting other genetic factors might be involved.

A litter of cats had a hair condition similar to a mouse mutation, leading to hair loss and abnormal hair and skin.

Lichen planopilaris may have a genetic link.

A 66-year-old woman's thick scalp and hair loss were confirmed as lipedematous alopecia, a rare condition possibly influenced by genetics, with no effective treatment known.