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Giving immune serum from vaccinated mice to mice without T cells prevents infection and tumor growth.

Boron neutron capture therapy for head and neck cancer can cause side effects like mouth sores and skin irritation, which vary depending on where the treatment is aimed.

"Moth-eaten alopecia" can be a sign of secondary syphilis, treatable with penicillin.

JAK inhibitors and platelet-rich plasma show promise for treating alopecia areata.

Too much vitamin A can cause liver damage and skin issues.

It's unclear if COVID-19 vaccination causes SLE; more research is needed.

Monilethrix is a genetic disorder causing brittle hair, diagnosed using tricoscopy.

FOXN1 gene mutations cause a rare, severe immune disease treatable with cell or tissue transplants.

The rash resolved after stopping ponatinib.

A 12-year-old girl was diagnosed with monilethrix, a genetic condition causing fragile, beaded hair that breaks easily, with no effective treatment available.

Carbamazepine may cause lung problems and lupus-like symptoms, which can improve after stopping the drug.

Tigason improved hair growth in a boy with monilethrix without side effects.

The donkey had a severe disease affecting multiple organs and was euthanized.

Anti-CD19 therapy may help treat SLE and NMOSD.

A woman had a rare skin condition with recurring painful nodules that heal in 6 weeks, often without needing treatment.

Non-motor symptoms in myasthenia gravis are common and need early diagnosis for better management.

The mtDNA N haplogroup is linked to a higher risk of late-onset lupus and specific symptoms in Han Chinese women.

A possible link exists between minimal change nephrotic syndrome and complete hair loss.

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

Acute leukemias with the Philadelphia chromosome may be biphenotypic, and identifying this is important for proper treatment.

Trichodysplasia spinulosa is a rare skin condition caused by a virus, treatable with antiviral medication.

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

SLE patients need careful diagnosis to distinguish infections from disease flares for proper treatment.

Two siblings had a rare immune disorder caused by a FOXN1 gene mutation.

A rare skin condition linked to leukemia improved with chemotherapy.

NEMO syndrome and systemic lupus erythematosus are linked in a new disease association.

A man with four autoimmune diseases suggests a new category for multiple autoimmune syndrome.