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NIR-II imaging effectively tracked stem cells that helped repair facial nerve defects in rats.

Monilethrix is not caused by a metabolic defect.

Surgical removal of eyelid mass showed it was non-cancerous, with no recurrence after one year.

A Chinese man with KID syndrome had a new mutation in the GJB2 gene.

Msx2 deficiency in mice leads to bone growth and organ development problems.

An 8-year-old boy with Recklinghausen's Disease shows various symptoms and is from a family with close genetic ties.

lncRNA XLOC_008679 and gene KRT35 affect cashmere fineness in goats.

A man's unusual scalp folds caused by a skin condition were treated with surgery and remained unchanged two years later.

A cat in Brazil had severe skin issues worsened by improper treatment.

A 16-year-old boy's facial condition improved with doxycycline, suggesting an immune response to hair follicle damage.

Albendazole treatment for echinococcosis can cause serious side effects and requires close monitoring.

Argentine-cross polo ponies commonly develop sarcoid tumors with distinct types and histopathological features.

The skin condition Ulerythema ophryogenes did not improve with treatment in a patient with other birth defects.

A new treatment for hair loss uses tiny lipid carriers to deliver a mix of minoxidil and latanoprost directly to hair follicles, promoting hair growth and being well tolerated by the skin.

Male Pomeranians with woolly coats are more likely to develop alopecia X.

'Eclipta prostrata' plants in Taiwan are infected with 'Candidatus Phytoplasma aurantifolia'.

The conclusion introduces a new way to classify skin cysts using their shape and genetic markers.

The Lanceolate hair-J mutation in mice mimics human hair disorders like Netherton's syndrome.

A 7-month-old girl with a rare skin disorder died because diagnosis was delayed.

A woman's scalp nodules were successfully treated with antifungal and anti-lice medications, revealing a rare case of mixed piedra infection.

Methylene blue staining effectively reveals detailed nerve structures in rat snouts.

A patient with a rare chromosome condition also had a rare type of hair loss.

Naltrexone shows promise as a safe treatment for a type of hair loss called lichen planopilaris.

The epicardium is vital for heart repair and regeneration, offering potential for new heart disease therapies.

Euph E and Euri A from Euphorbia neriifolia help control inflammation and immune response in cells.

CaBP1 and CaBP2 are necessary for proper hearing and neurotransmission in the ear's inner hair cells.

CaBP1 and CaBP2 are necessary for proper hearing and neurotransmission in the ear's inner hair cells.

HOXC13 is essential for hair and nail development by regulating Foxn1.

New technologies in acupuncture and biosensors show promise for better medical treatments and healing.

The protein FLCN is involved in cellular cleanup and is regulated by ULK1.