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A woman's hair loss and skin discoloration were found to be caused by a rare case of leprosy on the scalp, not alopecia-vitiligo overlap.

Vinblastine and its metabolites may cause nausea and hair loss by binding to specific receptors and could lead to better chemotherapy drugs with fewer side effects.

M-CSF-stimulated myeloid cells can cause alopecia areata in mice.

Topical patidegib gel effectively treats basal cell carcinoma in Gorlin syndrome patients without causing the side effects seen with oral treatments.

A new gene mutation linked to KID syndrome was found, expanding genetic knowledge.

People with alopecia areata have fewer IL-10 producing immune cells, which might contribute to the condition.

A specific gene change is linked to severe hair loss.

A new genetic mutation causing Xeroderma Pigmentosum was found in an 8-year-old girl, affecting her DNA repair.

The nodule on the woman's back was a benign hair follicle tumor, not cancer, but needed removal.

Arab APS1 patients have unique and recurrent AIRE gene mutations.

Mutations in the LIPH gene cause woolly hair in a child.

A rare skin condition in a boy is likely due to a specific genetic mutation pattern.

BMI1 is essential for preventing hair greying and maintaining hair color.

Malt1 protease is essential for regulatory T cell function and could be targeted to boost antitumor immunity.

Baricitinib improved hair loss and arthritis in a lupus patient.

Pilomatricomas don't follow the usual hair follicle cell differentiation process.

A specific gene mutation causes monilethrix in this family, and minoxidil treatment improves hair condition.

Different mutations in the 5 alpha-reductase-2 gene were found in affected individuals in the Dominican Republic, suggesting no common ancestry.

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

Kidney cancer cells without folliculin are more sensitive to radiation due to increased self-eating cell death.

Certain gene variations are linked to alopecia areata.

Lenalidomide helps hair follicle stem cells turn into melanocytes, which may improve repigmentation in vitiligo.

Cells lacking the Bax protein can outcompete others, leading to better tissue repair and hair growth.

Mutations in the p63 gene affect skin adhesion, barrier integrity, and hair growth.

Researchers found a new ABCD1 gene mutation linked to a rare brain and nerve disorder with unusual brain changes.

A new genetic mutation in the TRPV3 gene causes Olmsted-like syndrome in a Mongolian family.

MITF+ melanoma patients are more likely to have multiple melanomas and unique skin patterns.