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The early genes of a specific virus can cause abnormal skin cell growth and hair follicle changes.

The DQB1*03 allele is linked to higher alopecia areata risk in Italians.

The study suggests a link between varicella-zoster virus and segmental vitiligo, with evidence of the virus disrupting skin pigment cells.

A rare case of a transplant patient developing a skin condition linked to HPV-49.

A rare genetic disorder causes sparse hair and vision loss due to a CDH3 gene mutation.

Inhibitors of 11β-HSD1 show potential for treating type 2 diabetes but require more testing for safety and effectiveness.

Hepatitis B virus exposure may be linked to increased risk of alopecia areata.

A boy's hair loss and bone issues improved with specific vitamin D treatment and calcium.

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

A new HRAS gene variant may cause a range of symptoms including intellectual disability and psychiatric issues.

Hirsute women have lower type 2 17β-HSD enzyme levels, which improve with treatment.

A Taiwanese patient had hair loss and skin bumps without the usual gene mutation, suggesting other genetic factors might be involved.

Monilethrix is linked to the type II keratin gene on chromosome 12q13.

A specific gene variant may increase the risk of developing Alopecia Areata.

A gene deletion causes the "hairless" trait in Iffa Credo rats.

Adults with Tatton-Brown-Rahman syndrome may have serious heart problems and need lifelong heart monitoring.

Innate lymphoid cells type 1 may contribute to alopecia areata by damaging hair follicles.

Certain mutations in the hairless protein disrupt its ability to regulate the hair cycle.

DDR-II hair follicle cells don't respond to 1, 25-dihydroxyvitamin D3, aiding diagnosis.

The HtrA1L364P mutation causes brain dysfunction and blood vessel damage.

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

Targeting specific T cells may help treat alopecia areata.

A mutation in the iRhom2 gene causes hairless mice due to abnormal hair follicle development.

Type B Insulin Resistance Syndrome is rare, linked to lupus, and hard to treat due to severe insulin resistance.

A man developed excessive hair growth after treatment with interferon-alpha and ribavirin for hepatitis C.

A new mutation in the KRT86 gene was found to cause the hair disorder monilethrix in a Han family.

Researchers found a new mutation in the HR gene causing hair loss and skin bumps in a Pakistani family.

A genetic mutation in the LIPH gene causes a rare hair disorder with sparse, curly hair.

Dermal IgA deposition without symptoms is rare in Dermatitis herpetiformis risk groups.