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LHX2 and SOX9 identify unique hair follicle cell groups, crucial for hair maintenance.

Corneodesmosin is crucial for skin and hair health, and its dysfunction can cause skin and hair disorders.

Enhanced stem cells from the placenta can reduce fat cell formation in eye disease.

A new method accurately classifies hair types, showing global hair diversity.

A child with Sweet syndrome was found to have chronic granulomatous disease and improved with treatment.

A 24-year-old woman had a rare ovarian tumor that caused male-pattern hair growth and was hard to diagnose and treat.

A specific gene mutation causes Olmsted syndrome.

The trichohyalin gene is located at chromosomal region 1q21 with other skin-related protein genes.

Olmsted syndrome can be inherited as an autosomal recessive trait due to a rare TRPV3 gene mutation.

Mutations in the CYP21A2 gene are not a major factor in causing PCOS.

A woman with a new PTCH gene mutation has both Gorlin syndrome and severe hair loss.

People with androgenetic alopecia (AGA) have lower hair density and more single-hair units compared to those with normal scalps.

A new model helps predict treatment success in girls with early puberty.

Patients with alopecia areata should be checked for muscle spasms, diarrhea, and ANA to avoid missing Satoyoshi syndrome.

Desmocollin 1 and 3 have distinct patterns in human tissues, with Dsc1 in specific skin and hair layers and Dsc3 in various epithelial layers.

Certain mouse strains develop a skin condition similar to a human hair loss disease due to genetic defects.

Tjalma Syndrome is a rare condition in people with lupus, causing fluid buildup and high CA-125 levels, but not due to tumors.

A new mutation in the DCAF17 gene was found to cause Woodhouse-Sakati syndrome in a large family.

SPIOMET therapy may be a promising alternative to oral contraceptives for treating adolescent PCOS.

A 90-year-old woman's hand lesion was a rare, aggressive skin cancer treated successfully with surgery.

Japanese women's curved hair has an uneven internal structure and varied amino acid composition.

Congenital triangular alopecia is a harmless, non-spreading hair loss condition often seen in young children.

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Glycol chitosan hydrogels enable quick, safe 3D cell spheroid formation for various applications.

Uncombable hair syndrome causes dry, frizzy hair that can't be combed flat, seen in a young child.

A new compound effectively inhibits human 5α-reductase 1.