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A woman with Degos disease managed her condition for nine years with medications and had two healthy pregnancies, while a separate finding suggests a possible link between female pattern hair loss and high blood pressure.

A new gene variant in the DSP gene is linked to a unique type of hair loss.

JAK inhibitors may reduce depression in people with alopecia areata.

JAK inhibitors show promise for treating various skin disorders effectively and safely.

A woman with undifferentiated connective tissue disease was diagnosed with renal amyloidosis and carpal tunnel syndrome.

Ruxolitinib treatment led to unexpected hair regrowth in a patient with alopecia universalis.

Tofacitinib successfully treated vitiligo in a patient with lupus without side effects.

Sorafenib may cause hair loss in a way similar to alopecia areata.

A new genetic mutation causing Werner's syndrome was found in an Indian man.

Upadacitinib effectively treated severe hair loss in a child.

Recognizing CVG can help diagnose systemic amyloidosis early.

A genetic mutation in the SGK3 gene causes hairlessness in Scottish Deerhounds and may relate to human hair loss.

A 12-year-old girl was misdiagnosed with alopecia areata but actually had a nevus sebaceus with a genetic mutation.

A new mutation in the K6b gene caused a girl's late-appearing nail condition.

JAK inhibitors effectively regrow hair in children with alopecia areata and are safe to use.

Ruxolitinib can help regrow hair in severe alopecia areata.

JAK/STAT inhibitors show promise for skin diseases but aren't yet approved.

Janus kinase inhibitors show promise in treating alopecia areata but need better topical formulations.

Living with lupus as both a patient and doctor improved understanding and care for others.

Prednisolone improved symptoms in a woman with Cronkhite-Canada syndrome, but regular screenings are needed due to cancer risk.

Irish dermatologists urgently need guidelines for using JAK inhibitors in treating alopecia areata.

A rare case of severe scalp hair loss and nail issues in keratosis follicularis was observed.

Rhupus is a complex syndrome that combines rheumatoid arthritis and lupus, making diagnosis challenging.

Purpura fulminans can signal underlying autoimmune disorders, not just infections.

A 13-year-old boy with a rare genetic condition survived a heart attack and improved with treatment.

Early recognition of skin lesions in Birt-Hogg-Dubé syndrome is crucial for detecting renal tumors early.

A child with skin and heart issues had rare genetic mutations affecting skin and heart cell cohesion.

JAK inhibitors may soon be a safe and effective treatment for alopecia areata.

Alopecia areata is a complex condition causing hair loss, linked to genetics and immune system issues, and may be related to other autoimmune diseases; treatments vary in effectiveness.

Over 67 genes linked to ichthyosis help improve diagnosis and treatment.