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A rare skin reaction from cancer treatment was successfully managed with topical treatments and antihistamines.

A woman with lupus developed rare skin growths that went away on their own.

N-Cadherin is crucial in scar formation, offering potential for scar prevention therapies.

Nagashima-type palmoplantar keratosis in Asians is caused by a SERPINB7 gene mutation.

Ruxolitinib significantly improves multiple autoimmune conditions in APS-1 patients.

A man developed skin lesions as a side effect of a gamma secretase inhibitor used for treating a tumor.

A patient with advanced kidney cancer and no hepatitis C developed skin inflammation due to a drug called interferon alpha-2a.

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

Digital gangrene can be an initial symptom of late-onset systemic lupus erythematosus.

A woman developed a severe skin reaction from the antibiotic cefalexin.

These hair loss conditions might be part of a spectrum, not separate issues.

A woman with CHILD syndrome showed skin abnormalities, and the report suggests CHILD nevus and NEVIL might be the same condition, highlighting the need for diagnosis for genetic advice.

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

Rituximab leads to longer remission and fewer side effects than cyclophosphamide.

Mycophenolate mofetil is effective for treating severe lupus nephritis in children.

Immune checkpoint inhibitors can cause scalp inflammation and hair follicle issues.

EPDS can cause recurring scalp sores and hair loss if not treated.

Erythema nodosum linked to kerion can be treated effectively with antifungals and steroids to reduce scarring.

NIPP1 is important for healthy skin and could help treat skin inflammation.

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

A woman experienced severe side effects from a drug due to a specific genetic variation, suggesting genetic testing could prevent such risks.

The NIPAL4 mutation c.527C>A is common in Romanian patients with autosomal recessive congenital ichthyosis.

SJS/TEN survivors often have severe, overlooked long-term physical problems that are not properly treated after leaving the hospital.

Accurate diagnosis of NLS with dilated hair follicles is crucial to distinguish it from other conditions.

Digital gangrene can be a rare first sign of late-onset systemic lupus erythematosus.

Consider necrolytic acral erythema in similar cases and treat with oral zinc sulfate.

Dermatopathia pigmentosa reticularis causes skin discoloration, hair loss, and nail problems.

Gefitinib can cause hair loss without scarring.

Most children with childhood-onset lupus in Baghdad responded well to treatment, but some developed chronic kidney disease or died.