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The TRPV3 channel structure changes linked to severe itch and hyperkeratosis were identified using cryo-EM.

The four patients have a unique type of ichthyosis affecting hair follicles.

A 21-year-old with lichen planopilaris was successfully treated, stopping disease progression and preventing crusts.

A rare genetic skin condition usually affecting males was found in a 9-year-old girl.

The study found that males with KFSD had severe skin and eye symptoms, while female carriers had milder symptoms.

Ultraviolet techniques help identify Grover’s Disease, which may be underdiagnosed in young people and females.

Bullous pemphigoid can look like erythema multiforme, so awareness is needed for proper treatment.

People with keratosis pilaris might be more likely to get a rare type of tinea versicolor.

Keratins K6 and K16 are expressed more freely in regenerating mouse skin than K1 and K10.

The term "Porokeratotic Adnexal Ostial Nevus" is suggested as a more appropriate name.

Pachyonychia congenita is linked to a keratin gene on chromosome 17.

Treatment improved scalp conditions and hair loss with no recurrence after 1 year.

A rare skin condition with dark, thick, warty patches and some hair loss was found in a newborn boy.

Reducing immunosuppression and using antiviral creams improved the woman's skin condition.

A rare scalp condition called Erosive pustular dermatosis is hard to diagnose and treat.

A woman with HIV had a severe skin condition that improved with antiretroviral therapy.

The gene therapy showed significant wound healing and was safe for treating severe RDEB.

Peeling skin syndrome was successfully treated with a vitamin D cream.

Porokeratosis should be considered for scalp lesions, with new treatments like topical cholesterol/lovastatin offering promise.

A rare finger tumor was imaged, showing a unique pattern not seen before.

Brazilian keratin treatment can cause severe skin reactions.

Triptolide effectively and safely reduces actinic keratosis lesions in mice.

Trichostasis spinulosa is a common but often unnoticed skin condition involving bundled vellus hairs, especially in people with darker skin or UV exposure.

Erosive pustular dermatosis is a rare skin disease that's hard to treat and affects the scalp or legs.

Treatment with prednisolone and dapsone stopped new blisters and partially healed previous ones.

The skin condition Ulerythema ophryogenes did not improve with treatment in a patient with other birth defects.

Porphyria cutanea tarda causes skin issues due to an enzyme deficiency.

A man with scalp and neck skin issues improved after a year of oral isotretinoin.

A young woman with severe symptoms of CPAN improved with intensive treatment but needed a leg amputation.