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Three characteristics of plasmacytoid dendritic cells help tell apart lupus-related hair loss from LPP.

A man with a skin nodule was diagnosed with a rare skin condition called cutaneous focal mucinosis, which can be confused with other skin cancers.

A 30-year-old man with rare skin conditions improved with antibiotics and surgery, hinting at a link to rosacea.

Researchers found a potential new type of skin growth called follicular mucinous nevus.

Accurate diagnosis of APL is crucial to avoid unnecessary treatments.

Biopsy is crucial to correctly diagnose granuloma annulare, which can mimic other conditions like alopecia mucinosa.

The specific skin disease variant p.(Arg2000Trp) in plectin can cause a wide range of symptoms, which should be considered when diagnosing patients.

A rare skin condition in children can look like other diseases.

Hair loss in autoimmune blistering skin diseases varies and may regrow with disease control.

ALA-PDT is effective and safe for chronic X-ray dermatitis, providing complete or partial remission.

Accurate diagnosis is crucial for effectively treating severe alopecia and related symptoms.

BIVV009 is a safe treatment for bullous pemphigoid that reduces C3 deposition without harmful side effects.

Cutaneous lupus patients have higher levels of certain immune cells in their blood and skin.

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

A woman had a rare skin condition with recurring painful nodules that heal in 6 weeks, often without needing treatment.

Modulating the BTNL2 pathway can prevent hair loss in mice.

Dermoscopy helped diagnose a rare skin disease which slightly improved with treatment.

Natural killer cells play a key role in autoimmune skin diseases like pemphigus vulgaris.

The p.P25L mutation in the KRT5 gene causes a rare skin condition that worsens over time and may lead to hair loss starting in young adulthood.

Scalp involvement is common in pemphigus and can lead to hair loss, with the severity of scalp lesions linked to overall disease severity.

Pediatric pemphigus is often diagnosed late, but rituximab helps control it long-term.

Hair changes may indicate disease activity in pemphigus patients.

An 8-year-old girl developed a rare skin condition in a linear pattern on one side of her body after a lung infection, which improved with treatment.

Mutations in the p63 gene affect skin adhesion, barrier integrity, and hair growth.

Exosomes from Pinctada martensii mucus can safely reduce melanin production, offering a new treatment for skin pigment issues.

A bull with a gene mutation was asymptomatic, synthetic retinoids cause hair loss, and new therapeutic targets were identified for skin diseases.

Some skin growths with mucin can form hair follicles and resemble skin cancer, but a special stain can help tell them apart.

The upper hair follicle is stable, while the lower part allows movement during hair growth.

PLAU and SerpinB2 affect cell death differently in various forms of leprosy and could be targets for new treatments.