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LGR5 is a common marker of hair follicle stem cells in different animals and is important for hair growth and regeneration.

The grand round helps improve diagnoses and suggests new treatments for hair disorders.

Allopurinol may cause rare granulomatous microscopic colitis.

The first Japanese case of a genetic hair disorder caused by specific mutations in the LIPH gene was identified.

A genetic marker linked to a type of hair loss was found in most patients studied.

Cronkhite-Canada syndrome can be diagnosed without gastrointestinal polyps if there is severe mucosal atrophy and edema.

Vitamin D receptor may help protect against UV-induced skin cancer.

Early recognition and aggressive treatment can significantly improve rare ANA-negative lupus with heart and skin issues.

A rare genetic mutation caused unusual skin symptoms in a man with Blau syndrome.

5% topical minoxidil improves hair density and quality in monilethrix patients.

The 2012 criteria are better for diagnosing atypical lupus cases.

Mutations in the hairless gene cause hair loss and skin cysts in rhesus macaques.

hHb1, hHb3, and hHb6 mRNAs start expressing at the same time in hair follicles.

Colchicine can inhibit hair growth by affecting cell activity and protein expression in hair follicles.

The 308-nm excimer laser is a promising treatment for vitiligo with varying success and mild side effects.

Different types of PCOS in Chinese Han women show varying levels of male hormone and metabolic issues.

Cortisone reductase deficiency can cause high androgen and cortisol levels and may be missed in women with similar symptoms.

Topical minoxidil may help treat a rare genetic hair condition with no fully effective treatments yet.

A 16-year-old boy's facial condition improved with doxycycline, suggesting an immune response to hair follicle damage.

The ACE1 gene variant doesn't affect long-COVID symptoms.

Intralesional chemotherapy with 5-fluorouracil and methotrexate may worsen keratoacanthoma-type skin cancer in transplant patients.

A man with vitiligo and alopecia saw quick skin and hair improvement with ruxolitinib, but skin color gains were lost after stopping treatment.

The methylation of the HOXC8 gene's exon 1 affects cashmere fiber length in goats.

PCOS is likely inherited in families, increasing risk for first-degree relatives.

RNase L hinders hair growth by altering immune signals.

Skin of color can spontaneously repigment after a phenol-croton oil chemical peel.

rRSPO1 protein boosts hair growth by activating a key signaling pathway.

The 1298CC genotype in RA patients leads to higher methotrexate toxicity, while the 1298AA genotype results in better treatment response.

Testing for CAG repeat polymorphism in the androgen receptor gene is not currently recommended for managing hypogonadism.

Mutations in the ABCB6 gene cause Dyschromatosis Universalis Hereditaria.