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A specific mutation in the K25 gene causes a rare genetic disorder with curly hair at birth and later hair loss, along with dental issues.

Newly designed proteins can effectively degrade specific proteins in cells, offering a potential new therapy method.

PLLA dermal fillers can cause hair loss, but it can be treated with steroids.

Rezpegaldesleukin shows promise for treating severe alopecia areata.

Trichohyalin in sheep hair follicles may help with structure and calcium binding.

The gene LRRC15 is more active in balding areas of the scalp compared to non-balding areas.

A new gene mutation is linked to monilethrix in the studied family.

Alopecia areata involves immune system changes, especially in severe cases, with potential new treatment targets identified.

Pine resin and abietic acid were found to promote hair growth in mice.

A specific gene mutation causes complete hair loss in an Irish Traveller family.

Non-immune factors play a significant role in alopecia areata.

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

A man with rare skin changes on his fingers was diagnosed with multiple myeloma-linked amyloidosis.

Ritlecitinib shows promise for treating alopecia areata, especially with early and extended treatment.

Topical IKKα inhibitors may help prevent CCS tumours.

FGF-5 promotes Cashmere goat hair growth by increasing keratin genes and reducing certain LncRNA and target genes.

The skin of both rat strains showed similar lectin binding patterns.

A rare case showed alopecia areata and lichen planus occurring together in one person.

Topical putrescine and spermine increased DNA synthesis in hairless mouse skin.

Alopecia areata can be an early sign of Hodgkin’s lymphoma and may improve with lymphoma treatment.

Janus kinase inhibitors help some people with severe alopecia areata regrow hair, but not everyone responds, and relapses can happen.

Blocking TYK2 might be a new way to treat hair loss from alopecia areata.

Alopecia areata is linked to immune-related genes, suggesting JAK inhibitors as a potential treatment.

A new gene mutation causes a rare type of hair loss.

LTBP1 is a key regulator in diseases and a potential target for new treatments.

DM and AA may share a common cause.

CD80CD86 deficiency causes hair loss by disrupting regulatory T cells.

Intramuscular triamcinolone acetonide is an effective treatment for severe alopecia areata, especially in males.

Trichohyalin and peptidylarginine deiminase type III are found together in rat hair follicles, with trichohyalin being modified after expression.

A 2-year-old girl had a hair disorder not shared by her identical twin.