Search

everythinglearnresearchcommunity

for

Search:↓

A woman with a rare hair loss condition developed skin cancer in the bald area.

Over half of the children had abnormal hair under a microscope, with many having genetic hair conditions.

Trichoscopy can diagnose monilethrix, a genetic hair defect causing hair thinning and loss.

A single long white eyelash is a rare but benign condition.

Ruxolitinib can cause a delayed skin reaction on the nose.

Lichen planopilaris and frontal fibrosing alopecia are likely distinct diseases with different tissue involvement.

Cutaneous lupus erythematosus is a chronic skin disease that can progress to systemic lupus in some cases and requires treatment to prevent recurrences and scarring.

Aggressive SLE treatment helped hair regrowth and improved oral plaque, but scalp lesions stayed.

Two siblings have a rare genetic condition causing curly, coarse hair.

Dermoscopy is useful for diagnosing and monitoring discoid lupus erythematosus by showing specific skin patterns.

Temporal triangular alopecia may be linked to sebaceous nevus and shows a new pinkish background feature.

Spotted lunula may help identify alopecia areata.

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.