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TNFα and interleukin-1 blockers reduce skin inflammation from EGFR antibody therapy.

Early and accurate diagnosis is crucial for managing rare genetic disorders like this localized variant of junctional epidermolysis bullosa.

A new IL6ST gene variant may cause a unique form of hyper-IgE syndrome with skin abscesses and high IgE levels.

A genetic variant in the GJB6 gene likely caused the Labrador's paw pad condition.

AZD6244 treatment causes skin aging effects by depleting skin stem cells.

Visceral leishmaniasis can mimic rheumatoid arthritis symptoms, especially in immunocompromised patients.

Keloids can form at the site of a healed herpes zoster infection, but the reason is unclear.

Skin changes can indicate a risk for breast cancer.

A 38-year-old man was diagnosed late with Kearns-Sayre syndrome after being wrongly treated for epilepsy.

An 11-year-old girl with Kawasaki disease experienced hair loss that improved after treatment.

Recognizing the link between certain autoimmune disorders and neurological conditions can improve diagnosis and treatment.

A child's hair loss after Kawasaki disease may help understand the disease's autoimmune causes.

Keratoacanthoma changes as it grows, showing different hair follicle characteristics at each stage.

People with myotonic dystrophy type 1 tend to develop basal cell carcinoma at a younger age but not more frequently than others.

Thalidomide works best for skin lupus not helped by antimalarials, but has many side effects; other treatments are less effective, especially if patients also have systemic lupus.

Stromal cells in melanoma promote tumor growth and spread.

Netherton syndrome is a genetic skin disorder causing severe skin issues and requires careful treatment to protect the skin barrier.

Removing the liver tumor improved the patient's skin condition and hair growth.

Pediatric systemic lupus erythematosus is a severe autoimmune disease in children requiring early diagnosis and comprehensive management.

TNFα and interleukin-1 blockers reduce skin inflammation from EGFR antibody therapy.

Tailored treatment plans are crucial for managing canine dermatomyositis-like disease.

A 13-year-old girl with various symptoms was successfully treated for autoimmune disease using the antibiotic co-trimoxazole.

Immunocompromised patients can develop skin and hair issues due to a virus.

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

A woman with a new PTCH gene mutation has both Gorlin syndrome and severe hair loss.

Loss of a specific protein in skin cells causes symptoms similar to psoriasis.

XEDAR deficiency prevents muscle degeneration in EDA-A2 transgenic mice.

Restoring EDA and WNT pathways early may help improve skin, hair, and teeth issues in hypohidrotic ectodermal dysplasia.