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Alopecia in captive rhesus macaques is affected by season, sex, age, housing, and stress, with complex links between stress hormones and hair loss.

UV-enhanced trichoscopy helps diagnose hair shaft disorders like pili annulati.

Monilethrix is linked to the type II keratin gene on chromosome 12q13.

Young northern elephant seals with skin disease were smaller, had nutrient imbalances, and higher PCB levels, possibly linked to the disease.

A gene mutation worsens skin irritation in mice due to a lack of certain fats.

Eclipta alba extract improved learning, memory, and stress-related ulcers in rats without affecting movement or causing anxiety.

A 21-month-old boy has a rare genetic disorder causing sparse hair due to an LSS gene mutation.

Devon Rex cats with skin issues were successfully treated with antifungal medication.

Early diagnosis of Trichorhinophalangeal syndrome type 1 is crucial for treatment and was achieved through clinical examination and family history.

RHA fillers are effective and safe for treating nasolabial folds in people of color.

High selenium levels in some areas cause health issues in cows and buffaloes, but blood tests remain normal.

lncRNAs may help control cashmere goat hair growth by responding to light changes.

Peperomia pellucida is safe to eat and has strong antioxidant benefits.

Pili torti hair is fragile due to loose keratin filaments and weak disulfide bonds.

A multidisciplinary approach is crucial for treating complex cases of Rapunzel syndrome in children.

A Turkish family with sparse hair and eyebrow loss has a mutation in the U2HR gene linked to Marie Unna hereditary hypotrichosis.

These skin conditions in African men need combined medical treatments and lifestyle changes.

Genetic screening for NUDT15 polymorphisms is crucial for patients taking azathioprine, especially in Asians.

Ginsenoside Rg1 protects mouse skin from UVB damage and helps control inflammation.

Buffalo flies and Stephanofilaria nematodes cause severe skin lesions in beef cattle, and treatment should target both.

LHX2 is essential for hair follicle development, controlled by NF-κB and TGFβ2 signaling.

A Holstein calf in Iran with a severe genetic skin disorder was euthanized due to incurable symptoms.

Patients with certain FoxN1 gene mutations have severe immune issues but normal skin and hair.

Three siblings had both Vohwinkel's disease and congenital alopecia, with no effective treatment.

A boy with a new NR5A1 gene mutation has a sex development disorder without affecting his adrenal glands.

The child has a scaly rash and fever, but tests show no infection.

Fine needle aspiration with rapid on-site evaluation is useful for diagnosing pilomatrixoma.

A specific RNA helps increase the growth of skin cells in Liaoning cashmere goats by working with a protein to boost a growth-related gene.