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Skin symptoms in lupus help diagnose and manage the disease early.

Two new mutations in the CDH3 gene cause hair loss and vision problems in a young girl.

Mutations in the hHb6 gene cause the hair disorder monilethrix.

Recognizing unusual brain and skin symptoms is crucial for diagnosing lupus early.

Pediatric lichen is rare and diverse, and dermoscopy helps improve diagnosis and management in children.

High homocysteine levels in lupus may increase inflammation and cardiovascular risk.

Early detection and targeted management are crucial for better outcomes in systemic lupus erythematosus.

Glutamine may protect against alopecia areata, while certain cholesterol and glucose levels may increase risk.

An 11-month-old boy with Menkes disease had severe brain shrinkage and abnormal blood vessels, and didn't respond well to treatment.

A(1-7) treatment reduces symptoms of lupus in mice.

Dermatologists should recognize diverse discoid lupus signs to avoid misdiagnosis.

A rare skin condition called linear lichen planopilaris caused itchy red bumps and hair loss on a man's face.

Lupus patients in Ghana face healthcare challenges, and the Oyemam Autoimmune Foundation is working to improve awareness and support.

Undiagnosed lupus can cause severe complications after epidural anesthesia, leading to muscle weakness and potentially death.

A rare case showed basal cell carcinoma and leiomyosarcoma coexisting, needing careful diagnosis and treatment.

The PON1 192R gene variant is linked to a higher risk of psoriasis and heart disease in Western Mexico.

People with the same genetic mutation for Woodhouse-Sakati syndrome can have different symptoms.

Dietary lipids affect inflammation and are crucial for normal cell function and immune health.

Most Korean systemic lupus erythematosus patients experienced hair loss, often as non-scarring diffuse hair loss, with non-scarring patch alopecia also common.

Antituberculous drugs improved symptoms in a woman with lupus and myositis.

Lupus erythematosus can mimic alopecia areata, and trichoscopy is key for accurate diagnosis and better patient outcomes.

LONRF1 is important for oxidative damage response and tissue remodeling during wound healing.

Skin lesions in Carney Complex are caused by a gene change in some skin cells that leads to increased pigmentation and may lead to tumors.

Diagnosing and treating rapidly worsening lung disease is difficult and requires better guidelines and understanding.

Targeting specific metabolic and ionic pathways may improve alopecia areata treatment.

Leflunomide successfully treated a rare skin condition in a liver transplant patient.

PSENEN gene mutations can cause both Dowling-Degos disease and acne inversa.

A novel CLDN1 mutation in a 2-month-old with NISCH showed improvement with symptom management.

Early diagnosis and treatment of calcinosis cutis in lupus patients is crucial due to its rarity and potential complications.

Early diagnosis, intensive therapy, and careful follow-up are crucial for managing overlapping TTP and SLE.