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3D ultrasound can detect hair follicle changes and disease phases in alopecia areata.

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The 736T>A mutation in the LIPH gene is common in Japanese people with autosomal recessive woolly hair.

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Adalimumab significantly improves quality of life for patients with moderate to severe hidradenitis suppurativa.

All Indian dromedary camel breeds have the same KRTAP7 gene affecting hair quality.

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The KRTAP7-1 gene is very similar across different cattle and yak breeds and likely plays a role in hair strength and shape.

The DQB1*03 allele is linked to higher alopecia areata risk in Italians.

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

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A specific mutation in PA-PLA1α causes abnormal hair growth.

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Scientists developed a new way to study mutations in a skin condition using blood cells, which may help diagnose and treat the disease.

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

A genetic marker linked to a type of hair loss was found in most patients studied.

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Higher levels of CCL7 are linked to more severe hair loss in alopecia areata patients.

A genetic mutation in the hHa1 gene creates a smaller, but still functional, hair protein without causing hair problems.

Two new gene mutations cause a rare hair disorder.

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Farudodstat may help treat alopecia areata by protecting hair follicles.

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

ALUDWIG can help standardize female hair loss assessment from a single image.

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