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Mutations in the Vitamin D receptor gene can cause hair loss similar to mutations in the Hairless gene.

Prednisolone improved symptoms in a woman with Cronkhite-Canada syndrome, but regular screenings are needed due to cancer risk.

A new genetic variant causes trichothiodystrophy in two brothers, but their mother may carry it without showing symptoms.

Urtica dioica extract may help treat androgenic skin diseases by reducing a specific gene's activity.

Targeting NCoR1 can help treat heart enlargement and dysfunction.

Early shedding of the inner root sheath in noninflamed hair follicles is a relatively specific sign of Central Centrifugal Cicatricial Alopecia.

Hair sample weight is a better measure for cortisol levels in hair than hair protein concentration.

Stress can cause a type of hair loss in mice lacking the CCHCR1 gene.

Adrenocorticotropic hormone inhibits growth and affects body composition in male rats.

A woman with a unique syndrome similar to TRPS has a genetic change near the TRPS1 gene, affecting its regulation.

Researchers found a gene mutation responsible for a rare hair loss condition.

TrichoScan offers a painless way to analyze and manage hair loss.

CRTH2 antagonists might be useful for treating many conditions because they play a role in immune and inflammation responses.

Carpronium chloride increases blood flow by widening small blood vessels.

Alternating treatment with two drugs could help cells in a rapid aging disease.

Ritlecitinib helps regrow hair in people with alopecia totalis and universalis and is safe to use.

Researchers found key regions in the mouse hairless gene that control its activity in skin and brain cells, affecting hair follicle function.

Thrombophilic conditions may worsen Long COVID symptoms due to increased blood clotting.

Low-dose Ritlecitinib may help children with stubborn Alopecia Areata.

The C-terminal tail of AHF/trichohyalin is essential for organizing keratin filaments in keratinocytes.

rTMS may help treat trichotillomania in some patients.

A new genetic mutation in the CDH3 gene causes hair loss and eye problems in young people.

Researchers created rat liver stem cells that could help repair liver failure in rats and may be useful for studying human liver diseases.

New mutations in KRT83 and KRT86 are linked to the hair disorder monilethrix.

A person with a specific gene mutation had extra teeth, unique jaw and hair features not seen before in this condition.

CCCA is a hair loss type affecting African women, possibly caused by grooming and chemicals, with various treatments and needing more research.

Non-itchy rashes can indicate serious diseases like lupus.

Blocking certain immune signals can reduce skin damage from radiation therapy.

The trichohyalin gene is located at chromosomal region 1q21 with other skin-related protein genes.