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Mutations in specific keratin genes cause improper hair structure in mice due to faulty keratin protein assembly.

Carbon black nanoparticles can harm liver and kidney function in mice.

Researchers found a white halo around hair in most patients with a specific type of hair loss, which helps in early diagnosis and treatment.

Some masked palm civets in Japan have a skin disease caused by mites.

Cicatricial pattern hair loss is likely advanced common baldness, not a type of lichen planopilaris.

New RIPK4 gene mutations were found to cause a type of skin and limb birth defect.

Low vitamin C caused bleeding and corkscrew hair, resolved with vitamin C treatment.

CCC1 is essential for ion balance and proper plant cell function.

Mutations in the LIPH gene cause woolly hair in a child.

Long-term use of calcineurin inhibitors in transplant patients can cause hormone issues that can be managed with proper care.

A woman with myotonic dystrophy had multiple skin tumors on her scalp, suggesting a genetic link.

More research is needed on CCCA in children, especially Black and Asian adolescents.

Black women with CCCA are more likely to have uterine fibroids.

The report found a new type of hair loss in African-American women that affects more areas of the scalp than previously thought.

A 15-year-old with KID syndrome developed a rare skin condition called PEHFN.

Scientists found a new gene in a bacterium that can modify an immunosuppressant drug, potentially helping to treat hair loss.

The study found that Central Centrifugal Cicatricial Alopecia mainly affects middle-aged African descent women, is linked to certain hair care practices and genetics, and often goes undiagnosed for years.

A 2-year-old boy was diagnosed with a rare genetic condition causing fragile hair, intellectual issues, and short stature.

The TCL1 transgenic mouse model is useful for understanding human B-cell leukemia and testing new treatments.

Two new gene mutations cause a rare hair disorder.

Msx2-deficient mice experience irregular hair growth and loss due to disrupted hair cycle phases.

The horse had a rare disease causing weight loss and skin issues, leading to euthanasia due to poor treatment options.

Early detection and histopathology are crucial to prevent permanent hair loss in cicatricial alopecia.

Catatonia can be a rare sign of lupus, needing careful diagnosis and treatment.

The conditions alopecia areata, primary sclerosing cholangitis, and ulcerative colitis may be linked by shared autoimmune and cell death mechanisms.

Vitamin C deficiency harms both the body and brain, affecting behavior.

Blocking S100A8 can reduce chemotherapy-induced hair loss.

Polarizing light microscopy can easily and reliably diagnose congenital keratinizing disorders like Netherton syndrome.

Mite infestations severely harm the health of endangered Amargosa voles.