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Some brain cancer cells avoid immune system detection, and certain treatments could target this to slow their growth; also, certain fat cell precursors help regenerate hair and skin after injury.

A 42-year-old woman had a scalp lesion that didn't cause hair loss and showed specific changes under a microscope.

If someone has scaly skin, muscle stiffness, and intellectual disability, doctors should consider Sjogren-Larsson Syndrome, but other conditions if more symptoms are present.

A rare skin condition with dark, thick, warty patches and some hair loss was found in a newborn boy.

NISCH syndrome is a rare genetic disorder affecting skin and liver, with variable symptoms and limited treatment options.

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

A rare, harmless hair condition was found in an infant's eyebrow, needing no treatment.

Oral tofacitinib significantly improves lichen planopilaris symptoms without adverse effects.

A 12-year-old girl was diagnosed with monilethrix, a genetic condition causing fragile, beaded hair that breaks easily, with no effective treatment available.

Antifungal treatment can improve severe skin infections with cutaneous horns.

A rare benign skin growth called melanocytic matricoma was identified in a 69-year-old man.

Targeted therapy with Ustekinumab significantly improved a skin condition called ILVEN, which is caused by mutations in the CARD14 gene.

Lichen planopilaris is a chronic, scarring hair loss condition with no definitive cure, requiring accurate diagnosis and treatment to manage symptoms.

Early recognition and treatment of VATS in transplant patients improve outcomes.

CD8+ T cells attack hair follicle stem cells, causing scarring and hair loss.

Clouston syndrome is inherited in an autosomal dominant pattern and caused by a specific gene mutation, with no current treatment available.

Tigers had a skin condition causing hair loss and inflammation, but the cause is unknown and treatment didn't work.

Gefitinib therapy can cause unusual hair growth on the nose.

An 18-year-old man was diagnosed with a rare genetic disorder causing hair loss, severe light sensitivity, and skin issues.

Woolly hair syndrome is a genetic condition causing frizzy, fragile hair.

Lgr5+ stem cells do not cause skin tumors.

MFN2 mutations cause mitochondrial problems, unusual fat distribution, and low leptin despite high body fat.

Different types of scarring alopecia may be stages of one disease, and accurate diagnosis is crucial to prevent permanent hair loss.

The lentiviral array can monitor and predict gene activity during stem cell differentiation.

Lichen planopilaris can cause hair loss on limbs, not just the scalp.

Macrophages are more involved in Lichen planopilaris than in Frontal fibrosing alopecia.

Tinea capitis needs systemic treatment to avoid severe outcomes.