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Using travoprost for glaucoma may cause extra hair growth and darker skin around the eyes, but these effects can reverse after stopping the drug.

A gene mutation in mice causes skin defects and early death.

3D models from confocal microscopy improve melanoma detection on sun-damaged skin.

A new classification for trichothiodystrophy helps identify genetic causes and potential treatments.

Early biopsy is crucial for diagnosing rare skin sarcoidosis, improving treatment.

Gonadal hormones significantly affect the severity of alopecia areata in mice.

Harlequin ichthyosis involves abnormal skin cell structures and giant mitochondria, affecting skin and hair.

A brown shadow seen in dermoscopy is a marker for lichen nitidus.

The harlequin ichthyosis mouse mutation causes thick skin and early death, resembling a human skin disorder.

VKHD can include rare oral symptoms like discolored teeth.

Damaged hair follicles make mice more prone to skin inflammation and skin cancer after UV exposure.

Hair treatments cause significant structural changes, especially with excessive heat, regardless of ethnicity.

Green hair has high copper levels due to contaminated water and damaged hair cuticles.

Keratin structure changes during keratinization, but the exact model remains uncertain.

Trichoscopy, a hair loss evaluation technique, found that people with Androgenetic Alopecia have more thin hairs, yellow dots, and perifollicular discoloration than healthy individuals.

It's important to consider genetic hair disorders when diagnosing hair loss.

Oxidative dyes damage hair more than semi-permanent dyes, but new technologies help protect hair while coloring.

A specific gene mutation causes a severe skin disorder in a family.

A Turkish family with sparse hair and eyebrow loss has a mutation in the U2HR gene linked to Marie Unna hereditary hypotrichosis.

Trichothiodystrophy involves brittle hair due to low sulfur amino acids, not a transport defect.

Experience-dependent plasticity offers rehabilitation potential for macular degeneration, partial orthokeratology slows myopia, and axis misalignment affects astigmatism surgery effectiveness.

A new gene mutation causes complete androgen insensitivity in a 16-year-old with a female appearance.

Some medications can change hair color, especially chloroquine and cancer treatments.

An 8-year-old boy had both alopecia areata and vitiligo on the same spot on his scalp, which is very rare.

Trichothiodystrophy causes abnormal protein deposits and distortion in hair follicles.

The HCR gene contributes to psoriasis risk.

Maternal exposure to artificial food coloring may increase skin disease risk in rat offspring.

A mutation in the KRT71 gene causes a hair disorder by disrupting hair follicle structure and texture.