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A new mutation in the STING protein causes a disease with lupus-like symptoms and responds well to a specific inhibitor treatment.

A new genetic area linked to a rare hair loss condition was found on chromosome 13 in a Chinese family.

Truncated hHb1 keratin may play a role in breast cancer cell transformation.

Anti-MND antibodies are present in various diseases, not just PBC, and their levels don't correlate with disease activity or skin symptoms.

Common variants in the Trichohyalin gene are linked to straight hair in Europeans.

Certain CD8+ T cells attack hair follicles in alopecia areata, suggesting they could be targeted for treatment.

Mutations in the KLHL24 gene cause a skin disorder in some Russian families.

Hairless gene not strongly linked to baldness.

The E413K mutation in the hHb6 gene causes monilethrix, a hair disorder, but doesn't show consistent symptoms.

A man developed facial skin lesions after a stem cell transplant, which improved with specific treatments.

A neglected leprosy treatment led to rare scalp hair loss in an Indian woman, which improved with proper medication.

Researchers found a new area on chromosome 2 linked to a genetic hair loss condition.

Two gene variations, rs6493497 and rs7176005, may be linked to female hair loss in Chinese people.

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.

A Turkish family with sparse hair and eyebrow loss has a mutation in the U2HR gene linked to Marie Unna hereditary hypotrichosis.

In alopecia areata, certain immune cells increase and express a protein linked to immune activation.

JAK inhibitors can be safely used in alopecia areata patients with latent hepatitis B or tuberculosis, with proper monitoring.

The muscle damage was caused by T-cell large granular lymphocytic leukemia, not dermatomyositis.

A gene mutation in mice causes permanent hair loss and skin issues.

IFN-γ and IL-2 are important for T cell activation in hair loss in mice.

Lichen planus is a skin condition that can resolve on its own, is linked to hepatitis C, and increases the risk of skin cancer.

Certain IL-18 gene variations may increase the risk of alopecia areata.

A woman was wrongly diagnosed with lupus but actually had leprosy.

HDAC4 and HDAC7 are crucial for Th17 cell development and could be targeted to treat inflammatory diseases.

ULBP3 levels are higher in Tinea capitis patients and may help predict the disease's severity.

Vogt-Koyanagi-Harada disease can develop during interferon therapy for chronic hepatitis C.

Certain gene variations may increase the risk and severity of alopecia areata.

Relapsing hepatitis A can cause prolonged abnormal liver tests even without symptoms.

Some skin conditions are associated with other serious diseases, and office microscopy may miss many fungal infections.