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A genetic mutation in the LIPH gene causes tightly curled hair that stops growing in some Japanese individuals.

Some people with congenital triangular alopecia have a central tuft of hair in the bald patch, but the cause is unknown.

HIV-positive men who have sex with men have a higher rate of anal beta-papillomavirus infections.

A 59-year-old woman was diagnosed with a rare hair loss condition called lipedematous alopecia.

A 5-year-old girl got a rare case of extra hair growth on her arm after a henna tattoo.

A girl had two rare hair conditions that helped understand their overlap.

FAPD is a possible diagnosis for hair loss in patients of color and requires multiple evaluations for accurate diagnosis.

Genetic testing for hairless gene mutations is crucial to correctly diagnose and treat atrichia with papular lesions.

Scientists discovered two versions of a new human hair keratin gene.

A new compound from fermented papaya may help stimulate hair growth.

A cluster of sulfur-rich hair protein genes was found on chromosome 17.

A 9-month-old baby had a rare, persistent ring-shaped hair loss condition.

A rare combination of halo nevi, nonsegmental vitiligo, and early gray hair can occur together.

Using a scalp flap for hair transplantation gives denser, faster results than older methods, but it's complex and needs careful planning.

Congenital atrichia with papular lesions causes permanent hair loss and skin bumps from birth.

Isolated patchy heterochromia with pili annulati can occur without other health issues.

Researchers found a new mutation in the HR gene causing hair loss and skin bumps in a Pakistani family.

Scientists discovered a unique hair protein, KAP24.1, with a special structure, found only in the upper part of hair cuticles.

The study found that variations in hair protein genes are likely due to evolutionary deletions or duplications.

Blocking YAP/TAZ could be a new way to treat skin cancer.

Many Korean women with female-pattern hair loss have reduced hair density at the temples.

A new gene mutation causes a rare type of hair loss.

The new composite scaffold may effectively treat chronic and deep wounds.

HDPCM treatment healed a baby's congenital skin defect caused by varicella infection.

A 3-year-old boy was diagnosed with a rare, non-scarring hair loss condition called temporal triangular alopecia.

The method effectively analyzes human hair proteins, especially nonfilamentous ones.