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A woman with asthma improved from a severe fungal infection after treatment change, and most HIV-positive women in a UK study had low immune cell counts but were responding well to treatment.

Certain CD8+ T cells attack hair follicles in alopecia areata, suggesting they could be targeted for treatment.

A man developed a rare skin condition after a hair transplant surgery.

A specific group of early-stage melanocytes is reduced in vitiligo-affected skin, which may explain treatment resistance.

KLB and EIF3C genes are key for early diagnosis of vitiligo and alopecia areata.

The condition is likely inherited in an autosomal-dominant pattern.

Genetic differences affect COVID-19 severity and treatment effectiveness.

Most genetic mutations causing hypohidrotic ectodermal dysplasia in Russian patients are found in the EDA gene.

A rare skin condition called Eruptive Vellus Hair Cyst can cause itchy papules on the face.

Cell adhesion molecules are important in the development of certain skin diseases.

Follicular dystrophy in immunocompromised patients may be linked to medication or viral factors and can improve with treatment changes.

Revertant cell therapy could be a future treatment for Ichthyosis with confetti.

Alopecia areata involves complex immune dysregulation, mainly driven by Th1 activity, suggesting broader treatment strategies.

Some skin symptoms, like chilblain-like lesions, can help identify COVID-19 and show how the immune system is responding.

Early genetic testing and JAK inhibitors can help treat systemic inflammation in SAVI patients.

A rare genetic variant linked to skin cysts was found in blood DNA, suggesting its role in cyst formation.

Early diagnosis and teamwork are crucial for managing ILVASC effectively.

A new lab-grown lung model helps study adenoviruses and test antiviral drugs.

Vitiligo treatments are improving but relapses are common.

Most skin reactions to COVID-19 vaccines in India were mild and not a reason to avoid vaccination.

Careful monitoring is crucial to prevent JC virus reactivation in lupus patients treated with rituximab.

Using cidofovir cream for a rare skin disease can cause skin darkening.

Diffuse alopecia areata involves more inflammation and higher allergy-related antibodies than patchy types.

People with primary immunodeficiencies often have frequent, severe, or unusual infections and may need special tests and management strategies.

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

Certain gene variations in EGF and EGFR may increase the risk of alopecia areata in Koreans.

A new mutation in the STING protein causes a disease with lupus-like symptoms and responds well to a specific inhibitor treatment.

The trichohyalin gene is located at chromosomal region 1q21 with other skin-related protein genes.