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Damaged hair follicles make mice more prone to skin inflammation and skin cancer after UV exposure.

Sweat glands and hair follicles are determined by opposing signals, with BMPs promoting sweat glands and blocking BMPs leading to hair follicles.

Genetic testing confirmed a rare skin disorder in a young girl, which improved with zinc supplementation.

A 6-year-old boy's leg hair loss was due to friction from sitting cross-legged, and it usually resolves on its own.

Localized dystrophic epidermolysis bullosa (DEB) can lead to scarring alopecia, highlighting the need to recognize and address this complication.

Genetic testing for hairless gene mutations is crucial to correctly diagnose and treat atrichia with papular lesions.

A rare fungal infection caused hair loss in a North American infant.

Epidermolysis bullosa is a genetic disease causing fragile skin and blisters in both animals and humans.

Certain scalp patterns can indicate the severity and activity of hair loss in Turkish alopecia patients.

A person got uncombable hair syndrome from two copies of chromosome 1 from their mother.

A rare skin reaction from cancer treatment was successfully managed with topical treatments and antihistamines.

A mutation in the HOXC13 gene causes hair and nail problems in a Syrian family.

A family got a fungal infection from a boy who had contact with rabbits, but they all recovered with treatment.

Hair follicle bumps with stem cells might contribute to permanent hair loss by getting disconnected due to scarring.

Demodicosis should be considered in cats with facial skin issues exposed to inhalant glucocorticoids.

New gene variants were found for rare skin and hair disorders, improving understanding and treatment.

A sugar glider had a rare skin cancer that worsened despite treatment, highlighting the need for thorough checks in exotic pets.

New findings may help diagnose and understand scarring alopecia better.

Trichoscopy is a useful method for identifying primary cicatricial alopecias and their specific types.

A Doberman Pinscher had a rare form of autoimmune disease causing hair loss and other severe symptoms.

EGFR deficiency causes significant changes in skin cells and hair follicles.

A boy and his father with hereditary hypotrichosis simplex were treated for hair loss, but the treatment result is unknown.

Abnormal cuticle and hair shaft medulla cause hair loss in androgenetic alopecia; sonography helps diagnose and manage it.

Activated β-catenin affects hair growth and skin thickness, and changes are reversible.

A rare family case of multiple benign hair follicle tumors was identified, highlighting the need to distinguish them from similar conditions.

A 16-year-old boy's arm hair grew more after wearing a splint, but it returned to normal in 8 months.

Nail disorders are often related to jobs like housework and manual labor, with cosmetic issues being the main concern, and are commonly caused by skin diseases like psoriasis.

The man's scarring alopecia and skin issues did not improve with treatments.