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Clinical signs don't match inflammation levels in lichen planopilaris and frontal fibrosing alopecia.

The research found a way to identify and study skin cells with stem cell traits, revealing they behave differently in culture and questioning current stemness assessment methods.

Two unusual cases showed that Lichen Planopilaris can look like other skin conditions and need early treatment to protect hair.

A woman with a rare type of dermatomyositis improved with low-dose prednisone and methotrexate.

Topical tacrolimus can effectively treat erosive pustular dermatosis and related hair loss.

A 70-year-old woman with bronchiectasis developed a rare immune disease due to a bacterial infection, requiring a difficult balance of treatments.

Plica Polonica is a rare hair disorder causing severe matting, managed by detangling or cutting, and prevented with regular hair care.

Pilomatricomas are often linked to genetic syndromes, especially Apert syndrome, and genetic analysis is crucial for diagnosis.

A new mutation in the TRPS1 gene caused Trichorhinophalangeal syndrome in a 17-year-old, highlighting the need for genetic testing.

Overexpression of hurpin in mice leads to abnormal skin and higher skin cancer risk.

Diagnosing oral ulcers can be complex and requires careful examination and follow-up.

The placebo microneedle stamp didn't penetrate skin and caused less pain, but blinding was only effective for those with low skin sensitivity.

Dermoscopy helps doctors recognize a type of benign skin tumor called pilomatricoma.

A new mutation in the KRT86 gene causes a hair disorder with variable expression.

Consider necrolytic acral erythema in similar cases and treat with oral zinc sulfate.

Complex basal cell carcinomas need personalized treatment due to unique genetic mutations.

Targeting Hedgehog signaling may help treat ligamentum flavum fibrosis.

Kir6.1 mutations in Cantú syndrome increase channel sensitivity and hyperpolarization, while SUR2B mutations do not.

Merkel cells stabilize nerve endings in the skin, and they change independently of each other.

The pony's skin condition improved significantly with prednisolone treatment.

A rare hair disorder with multiple hairs from one follicle was found on a patient's abdomen.

Mitochondrial problems in diabetic nerve damage might cause pain by lowering the production of certain nerve-related steroids.

The flaky skin mouse mutation is a natural model for studying human psoriasis.

Coat-type differences in Pomeranians affect Alopecia X diagnosis and treatment.

Pilomatricoma is a rare, harmless skin lump that needs accurate diagnosis and timely treatment.

Using platelet-rich plasma with microneedling works better for acne scars than microneedling with water.

Genetic testing can help diagnose skin conditions but needs more research for full effectiveness.