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

Shiny white structures in trichoscopy can indicate long-standing discoid lupus erythematosus alopecia.

Trichorrhexis nodosa is mainly caused by hair trauma, not a metabolic defect.

The Thr1022Ala variant in the hairless gene is not a disease-causing mutation.

PUVASOL might effectively treat complete scalp baldness.

Trichofolliculoma was found in a person with amniotic band syndrome for the first time.

Consider TFI in facial hypopigmentation diagnoses and confirm with a biopsy.

Scalp pemphigus vulgaris can be effectively treated with low-dose prednisone and triamcinolone.

Researchers found a gene mutation responsible for a rare hair loss condition.

COVID-19 can cause hair to become progressively kinked.

A new mutation in the Hr gene causes hair loss in mice, similar to a human hair disorder.

Netherton's syndrome may have a familial link and doesn't always include atopy.

Removing MCPIP1 from myeloid cells in mice leads to hair loss and prevents skin tumors but causes pigmented spots.

Researchers found a new genetic mutation causing a rare hair loss condition in the first Japanese child studied.

A chromosomal change may cause ectodermal dysplasia and developmental issues in a child.

A deficiency in the TTC7A gene causes immune problems, gut issues, and hair loss.

A young child with alopecia areata and psoriasis improved with treatment, suggesting a link between the two conditions.

A 6-year-old girl had both monilethrix and trichorrhexis nodosa, causing brittle hair, with minimal improvement from treatment.

Treatment improved scalp conditions and hair loss with no recurrence after 1 year.

The mutant HR bmh protein mis-localizes in cells, affecting skin and hair development.

TRIV-509 quickly improves skin barrier and cell health in atopic dermatitis.

Mutations in the DSG4 gene cause specific hair and scalp issues.

Trichohyalin helps in hair and skin cell structure and function by binding calcium and linking proteins.

TTD symptoms vary widely, requiring thorough evaluations.

A gene mutation in mice causes permanent hair loss and skin issues.

Nagashima-type palmoplantar keratosis in Asians is caused by a SERPINB7 gene mutation.

Monilethrix is a genetic hair disorder affecting hair shape, seen in two brothers.

Cystic panfolliculoma resembles hair follicle tumors due to specific cell interactions.