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Tiny infundibular cysts are the main lesions in chloracne, not comedones.

A new gene mutation is linked to monilethrix in the studied family.

Fibre optic confocal imaging can visualize skin layers, blood vessels, and nerves in live mice.

Dirty dots are a common scalp finding in elderly women and can be washed away with shampoo.

Some medications can cause rare hair color changes, and reporting these side effects is important for patient quality of life.

Hair can show daily calcium changes, linked to body calcium levels and influenced by hormones, and can help assess calcium metabolism issues.

DNA phenotyping can predict physical traits like eye, hair, and skin color, improving forensic investigations.

A boy's scalp infection, usually found on the body, was effectively treated with antifungal cream.

SPRY1 deficiency in skin cells causes stem cells to move to the skin surface, leading to increased pigmentation.

Women with PCOS have thicker parafoveal areas in their retinas, but their macular blood vessel density is normal.

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

Thallium poisoning can cause serious eye problems and other severe health issues.

Early diagnosis and treatment of haemochromatosis are crucial for reversing organ damage and improving fertility.

Copper treatments increase copper in all tissues, but brindled female mice accumulate much more copper in their kidneys without clinical effects, unlike brindled male mice where brain copper deficiency is clinically significant.

The mutant HR bmh protein mis-localizes in cells, affecting skin and hair development.

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

Immature hair cells can grow and change into different types of hair cells over time.

Sensitive scalp has higher pH, more redness, abnormal sebum, and altered bacterial makeup.

Bleaching hair increases cysteic acid levels in a predictable way.

Hypothyroidism patients with hair loss typically have thinning hair, smaller hair follicles, and normal hair shedding.

Riboflavin with blue light speeds up hair dyeing, making it faster, safer, and long-lasting with less hair damage.

Yellow dots are common in severe alopecia areata.

Foxn1 is essential for hair pigmentation by directing pigment transfer to hair cells.

People with premature hair graying have an imbalance between harmful and protective molecules in their body, hinting that antioxidants might help.

The E413K mutation in the hHb6 gene causes monilethrix, a hair disorder, but doesn't show consistent symptoms.

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

Low hemoglobin levels are significantly correlated with hair loss in women with Telogen Effluvium.

Langerhans' cells are not responsible for depigmentation in this mouse model.

Recognizing mild or atypical cases of ectodermal dysplasia is crucial for better treatment and future planning.