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A new gene mutation causes vitamin D resistance and rickets, treatable with calcium therapy.

Baricitinib successfully regrew hair in an 8-year-old boy with alopecia totalis linked to a KRT74 gene variant.

KRTAP28-1 gene can help breed sheep with finer wool.

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

The research linked PLCD1 gene variants to the development of trichilemmal cysts.

A new keratin, hK6irs1, is found in all layers of the hair follicle's inner root sheath.

Nellore cattle have genetic variations linked to their adaptation to tropical environments.

Li2CO3 improved skin disease in a mouse model of Focal Dermal Hypoplasia without toxicity.

CXCL7 is essential for muscle repair by aiding early neutrophil infiltration.

Nocturnal calcium infusions improved a boy's severe rickets without causing hair loss.

Lack of functional CYLD in mice leads to early aging and cancer.

The new assay can help develop products for hair re-growth.

A man with both Klinefelter syndrome and primary hyperparathyroidism showed a rare combination of symptoms and genetic patterns.

Certain human skin cells marked by CD44 and ALDH are rich in stem cells capable of long-term skin renewal.

Double-stranded RNA activates a pathway that causes a skin protein to be expressed in the wrong place.

A patient with Cronkhite-Canada Syndrome developed colon cancer that spread to the liver, showing the need for regular cancer checks in such patients.

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

GI197111X is best dissolved in Capmul MCM for trials.

Researchers found that certain RNA circles in the brain are linked to disease risk, but their exact role in disease is still unknown.

A specific genetic trait in tumor cells is linked to longer survival without disease in certain lymphoma patients.

CRABP2 helps increase the growth of cells important for hair growth by activating a specific growth pathway.

Certain genetic variants in keratins increase the risk of tooth decay.

Prednisolone and Bactrim improved symptoms in a woman with Cronkhite-Canada syndrome.

A new mouse mutation causes skin and hair defects due to a gene change.

The L457(3.43)R mutation in the human lutropin receptor causes increased activity and hormone insensitivity, leading to precocious puberty.

A rare genetic mutation causes resistance to vitamin D, leading to severe rickets and requiring high doses of calcium and vitamin D for treatment.

Calcium blockers may help prevent hearing loss by protecting hair cells.

Retinoids can help reduce keratin buildup in skin conditions.