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The sponges effectively prevent dry socket by stopping bleeding and killing bacteria after tooth extraction.

Olmsted syndrome is a rare skin disorder causing thickened skin and other symptoms.

Recognizing Jacquet's sign helps diagnose and treat traction alopecia accurately.

Abnormal scalp whorls can indicate brain development issues but may also be seen in neurologically normal people.

The unique coat of lykoi cats is likely caused by new variants in the Hairless gene.

Hair follicles in the back of the rosette fancy mouse have reversed orientations due to a gene mutation.

The document concludes that understanding the evolution of the human face helps cosmetic surgeons meet aesthetic desires.

Netherton's syndrome may have a familial link and doesn't always include atopy.

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

A 5-year-old girl has lipoid proteinosis, causing voice issues, hair thinning, skin lesions, and tongue movement problems.

Recognize Rapunzel syndrome in children with unexplained stomach issues for timely treatment.

A new mutation caused a rare hair disorder in a Polish girl, not inherited from her family.

Hair follicle cells can help regenerate teeth.

Changing certain hairstyles can prevent worsening hair loss in Mexican women.

Natural hairline asymmetry should be embraced for better-looking hair transplants.

The lower part of rat vibrissa hair gets more blood and is well-protected for growth.

Monilethrix is a rare genetic hair disorder with no cure, but low-dose oral minoxidil may help.

Trichoscopy is good for telling apart tinea capitis and alopecia areata in kids.

Hair loss improved with treatment and successful transplant.

The EDAR gene mutation leads to thinner and more deformed hair shafts.

Her hair grew back normally after she stopped rubbing it.

A girl with Pitt-Hopkins syndrome developed curly hair as a rare side effect from the epilepsy drug perampanel.

Oxidized trichocyte keratin has a helical dislocation in its structure.

A KRT71 mutation in Hereford cattle in Uruguay causes thin, curly hair and scaly skin.

Recognizing specific features of African-American hair can help diagnose hair loss conditions.

A girl with Turner syndrome had psoriasis, alopecia areata, and trachyonychia.