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Early recognition and treatment of severe SLE symptoms can improve outcomes.

Two sisters had a rare hair condition without other usual symptoms.

Combining terbinafine and mitotane effectively treated a schnauzer's skin infection and hormone disorder.

A 9-year-old boy had a rare scalp condition usually seen in young men.

A bull with a gene mutation was asymptomatic, synthetic retinoids cause hair loss, and new therapeutic targets were identified for skin diseases.

The four patients have a unique type of ichthyosis affecting hair follicles.

A TNFAIP3 gene mutation can cause unusual and varied symptoms of lupus and Sjogren's syndrome.

Some family members had a condition with both loose hair and unique eye changes, possibly indicating a new type of ectodermal dysplasia.

A baby had a rare condition with abnormal blood vessels in the brain and unusual skin and hair growth, possibly a new syndrome.

A new mutation in the STING protein causes a range of symptoms and its severity may be affected by other genetic variations; treatment with a specific inhibitor showed improvement in one patient.