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Both HLA-B and MICA are independently linked to alopecia areata.

A family was found with both Trichorhinophalangeal syndrome and Loose Anagen Syndrome, suggesting a genetic connection.

Patients with myotonic dystrophy often have skin problems that suggest early aging and vitamin D issues, and the severity of these problems is linked to their genetic condition and vitamin D levels.

The harlequin ichthyosis mouse mutation causes thick skin and early death, resembling a human skin disorder.

Mutations in the TSPEAR gene cause a new form of ectodermal dysplasia affecting hair and tooth development.

A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

Matrical tumors share a common growth mechanism involving the Wnt pathway and consistent PHLDA1 expression.

Trichoscopy is useful for diagnosing Netherton syndrome in children with skin issues.

Mice with the naked gene have missing or abnormal hair cells.

Scientists can mimic hair disorders by altering genes in lab-grown human hair follicles, but these follicles lack some features of natural ones.