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BTNL2 helps protect hair follicles from immune attacks, which could aid in treating alopecia areata.

Baricitinib is effective and safe for severe alopecia areata, working similarly with or without an atopic background.

Biotin supplements improved skin and hair problems in a girl with biotinidase deficiency.

BFNB could be a promising treatment for hair growth.

Biotin treatment improves symptoms of biotinidase deficiency, but some neurological damage may be permanent.

Mice with damaged skin or hair follicles are more susceptible to anthrax infection.

BBR-SA nanomedicine is a safe and effective treatment for breast cancer.

Swedish men with the E213 A-allele of the androgen receptor have a lower risk of prostate cancer.

Changes in the SREBF1 gene cause a rare genetic skin and hair disorder.

SH-SY5Y cell lysate is effective for diagnosing Satoyoshi syndrome.

IFAP syndrome is a rare genetic disorder causing skin, hair, and eye issues, with limited treatment options.

The newborn was diagnosed with a rare skin disorder causing blisters, which requires careful wound care and family support.

Scalp hair follicle cells help protect and heal skin in certain skin conditions.

Biofeedback treatment for dysfunctional voiding in adults showed no symptom improvement.

NonClassic Congenital Adrenal Hyperplasia is a less severe form of a genetic disorder affecting adrenal gland function.

The grand round helps improve diagnoses and suggests new treatments for hair disorders.

PCA patients have more harmful bacteria and antibiotic resistance, needing specific testing for treatment.

A young Russian girl with Meier-Gorlin syndrome has two new mutations in the CDC6 gene.

Researchers identified promising inhibitors for the BRD4 protein, including finasteride and amentoflavone.

TAK-279 effectively reduces psoriasis symptoms and is safe.

Cantú syndrome may be linked to pituitary adenomas.

A new gene location for Keratosis follicularis squamosa was found on chromosome 7p14.3-7p12.1.

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

Hair shaft changes may be linked to CCCA, but their role is unclear.

A genetic variant in "Blonde d'Aquitaine" calves causes death at birth due to a missing protein.

The document reports the first Brazilian case of a girl with Becker nevus syndrome, characterized by skin changes, breast underdevelopment, and scoliosis.

A new type of pachyonychia congenita linked to a specific keratin gene mutation was found in two Pakistani families.

Baricitinib for severe alopecia areata is generally safe, with common side effects like infections and acne, and low rates of serious complications.

A bull with a gene mutation was asymptomatic, synthetic retinoids cause hair loss, and new therapeutic targets were identified for skin diseases.

Sex steroids affect the MafB gene differently in male and female hamsters.