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Curly and straight hair differ in how their internal fibers are arranged.

Folliculotropic mycosis fungoides can affect the central nervous system in advanced stages.

Two new gene mutations cause a rare hair disorder.

Onychomatricoma is a unique nail tumor, not related to other hair-related tumors.

A new mutation, Glu402Lys, in hair keratin is linked to variable symptoms of monilethrix.

Curly wool has more orthocortex than straight wool.

Keratinous tissues have multiple structural layers, including ordered keratin and lipid granules.

Mutations in the hHb6 gene cause the hair disorder monilethrix.

Trichoscopy can reveal specific hair and scalp changes in linear morphea.

Sheet formation is key to macrofibril structure differences in wool.

A 9-year-old girl has a rare hair disorder causing beaded, sparse hair.

Hair changes and a high occipital hairline may help diagnose Trichorhinophalangeal Syndrome.

A common mutation in the hHb6 gene is linked to monilethrix, but other factors may also play a role.

Polarized dermoscopy is slightly better than nonpolarized for diagnosing hair disorders, with each method having its own strengths.

The boy's hair and skin color differences are due to a pigmentation disorder.

The antibody created from BCC tissues reacts similarly to both BCC and hair follicles, suggesting BCC may come from hair follicle cells.

The study revealed the detailed structure of a keratin dimer, aiding understanding of how intermediate filament proteins function.

A new mutation in the KRT86 gene causes monilethrix in a Han family.

A new genetic mutation in the TRPV3 gene causes Olmsted-like syndrome in a Mongolian family.

A 4-year-old girl had a rare hair disorder affecting only part of her scalp.

A family showed a new condition with inherited hair loss and skin changes, possibly due to one genetic disorder.

Hair follicle patterns form through a mix of self-organization and signaling interactions.

The new system helps detect and track early female hair loss better.

Zouboulis syndrome is a rare condition that helps diagnose monosomy 18p early.

HKN-2 antibody targets specific skin and hair cells, showing keratin complexity.

Trichoscopic examination is crucial for diagnosing congenital triangular alopecia.