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Mutations in the AR gene cause hair thinning and loss.

Mutations in the ACTB gene cause Becker’s nevi and may lead to muscle issues in Becker’s nevus syndrome.

The brow-suspension suture is a quick, safe, and effective alternative to traditional brow lifts.

A painless cheek lump was misdiagnosed but found to be a rare, benign skin lesion called pilomatrixoma, treatable by surgery.

SK2 channels help control sensory signals in rat muscle spindles and hair follicles.

A new mutation in the PLEC gene causes a rare condition with skin blistering, muscle weakness, and hair loss.

PEA boosts allopregnanolone production and reduces oxidative stress in brain cells.

Powered exoskeleton training improves body perception and quality of life in spinal cord injury patients.

Using truncal anesthesia on the supraorbital nerve reduces pain in hair loss treatments and improves patient comfort.

People with palmoplantar pustulosis, especially with bone issues, have different mouth bacteria compared to healthy people.

A woman's scalp nodule was a common, harmless pilar cyst, treated by surgical removal.

Pilomatrixoma is a rare, harmless tumor near the eyebrow in kids, best treated with surgery.

Human sweat glands contain stem cells capable of self-renewal and forming different cell types.

Pilomatricoma is a rare, harmless skin lump that needs accurate diagnosis and timely treatment.

Palmaris longus muscle absence is uncommon and not linked to gender, hand side, or finger ratio.

Muscle-only free flaps for skull coverage have more long-term complications than composite flaps.

Surgeons should know about pilomatricoma for accurate diagnosis, even though it's rare.

Neuromyotonia and morphoea can occur together in the same body areas.

Stem cells in eccrine glands could be used for regenerative medicine.

Lambertianic acid helps prevent muscle wasting.

Dermoscopy helps diagnose unusual skin lesions like osteonevus of Nanta and can prevent misdiagnosis of serious conditions.

The dermal sheath's contraction is crucial for hair follicle regression and stem cell relocation.

SSEA-4 can distinguish between eccrine and apocrine sweat gland ducts.

The silver marmoset's skin is thin, lacks pigment cells, and has unique features like keratinized spines and specialized glands.

The study concluded that the new wound model can be used to evaluate skin regeneration and nerve growth.

Dandruff and seborrheic dermatitis are caused by yeast feeding on scalp oils, leading to irritation and flaking.

A new mutation in the Connexin 26 gene was found in a patient with KID syndrome, expanding the known disorders linked to this gene.

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

Fingerprints form uniquely before birth due to specific genetic pathways and local signals.