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Nandrolone phenylpropionate injections thickened the skin and enlarged oil glands in female hairless hamsters.

The ferret had a malignant apocrine gland tumor and did not survive surgery.

Hirosaki hairless rats have sparse, twisted hair due to missing hair keratin genes.

A new genetic mutation causes severe Leydig cell hypoplasia, affecting sexual development.

Canine hair follicles have stem cells in the bulge region.

Researchers found that certain lipids, especially vitamin D3, are lower in prematurely grey hair than in pigmented hair.

Murine hair has specific types of ceramides and glucosylceramides but lacks acylceramides.

Cronkhite-Canada syndrome may be more treatable and less severe than previously thought.

A dog had a rare skin tumor called desmoplastic tricholemmoma.

Cronkhite-Canada syndrome causes chronic diarrhea and has a poor prognosis despite treatment.

New mutations in hair keratin genes cause the rare hair disorder monilethrix.

A new gene mutation linked to a skin condition was found in a Spanish family.

A 14-year-old girl with no menstrual period was diagnosed with Swyer Syndrome and treated for a related cancer risk.

Becker's Nevus Syndrome is a rare condition with a skin patch and possible bone and muscle abnormalities, treated mainly for appearance.

There is no standard treatment for the rare Cronkhite–Canada syndrome, which can be fatal and lead to cancer.

A 72-year-old man with sudden taste issues and hair growth was diagnosed with a severe stomach cancer and died within 5 months.

Epidermolysis bullosa in calves was not caused by mutations in the keratin genes bKRT5 and bKRT14.

Hair root analysis can effectively detect somatic mosaicism in double cortex syndrome.

Defective protein folding due to a mutation is key in ANE syndrome.

A woman with a rare hormone resistance condition also had missing teeth and hair loss, which might be new symptoms of her genetic disorder.

The Indian buffalo teat has a melanin-rich epidermis, no hair follicles, and a complex structure with muscle, blood vessels, and immune cells.

A teenager's hair with alternating white and dark bands, known as Pili annulati, is a genetic condition that is usually harmless and often considered attractive.

Cellular debris sticks to damaged wool fibers and affects wool cleanliness.

Immunochemotherapy successfully treated neutropenia in a patient with Waldenström's macroglobulinemia.

Elderly patients with eruptive skin bumps may have clear cell syringoma linked to glucose issues.

K31 can identify clear secretory cells in human sweat glands.

A woman had a skin condition with increased normal elastic fibers, not related to other known disorders, likely due to aging.

A rare pigmented skin tumor called melanotrichoblastoma was diagnosed in a 51-year-old woman.

Norfolk Terriers have a genetic skin defect causing scaling and blisters due to a keratin issue.