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Low fluence photoepilation temporarily removes hair by targeting the hair follicle's pigmented area without severe damage.

15-Gy x-ray irradiation temporarily alters rat calvaria skin without causing significant inflammation or fibrosis.

Mutations in the KLHL24 gene cause skin blistering in epidermolysis bullosa simplex.

Alopecia areata patients show unique protein activity patterns, suggesting imbalanced signaling pathways.

Steroid injections improved symptoms and hair regrowth in a woman with a reaction to permanent makeup.

A specific gene mutation causes sparse, brittle hair in a family.

Hair root sheaths are more common in non-scarring hair loss and help diagnose the type of hair loss.

Both induced and spontaneous AA lymphocytes can cause alopecia areata in mice.

A brown shadow seen in dermoscopy is a marker for lichen nitidus.

The growth of the Epstein-Barr virus in the patient's cells was linked to the worsening of her lymphoma.

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

A woman with scalp lymphoma and hair loss improved with radiotherapy, highlighting the need for biopsies in similar cases.

Monochromatic light devices, especially the 308-nm excimer laser, are promising for treating alopecia areata but more research is needed.

The same genetic mutation in Sjögren-Larsson syndrome can lead to different levels of severity, suggesting other factors influence the symptoms.

Omalizumab may cause temporary hair loss, especially in women aged 18-60.

Lipid-antigen stimulation may play a role in folliculotropic mycosis fungoides.

A new mutation in the KRT86 gene causes monilethrix in a Han family.

Gamma-ray exposure during hair rest phase harms hair growth and color in mice.

The cross beam laser is a useful tool for safely measuring scalp stretchiness to improve hair transplant results.

A new mutation in the CDH3 gene causes hair loss and vision problems in a young girl.

A rare skin condition usually on the face was found on a man's heel.

A genetic region near the PAX1 gene is linked to a higher risk of scoliosis in females.

Patients with alopecia areata should be checked for muscle spasms, diarrhea, and ANA to avoid missing Satoyoshi syndrome.

A woman with a rare autoimmune disorder had a blister on her eye and unique immune reaction, which was effectively treated with medication.

A rare skin condition causes red, dark, bumpy facial lesions.

The hydrogel helps heal wounds without scars by releasing two drugs gradually.

Yellow dots are common in severe alopecia areata.

Some domesticated animals have the same genetic skin diseases as humans, which can help doctors understand human genetic mutations.

The method effectively images and correlates elements and metabolites in tissue samples at a micron scale.