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A gene variant increases the risk of a type of hair loss by affecting hair protein production.

Scientists discovered a unique hair protein, KAP24.1, with a special structure, found only in the upper part of hair cuticles.

Larger nail cavity sizes suggest benign tumors, while smaller ones may need further biopsy to rule out cancer.

PAON shows skin patterns due to genetic mosaicism.

A benign skin tumor grew quickly in a dialysis patient and was surgically removed.

An adult with a rare skin condition improved with tazarotene treatment.

Breast cancer alters specific molecular structures in hair, which revert after cancer removal.

Laser treatments are the most effective for porokeratotic adnexal ostial nevus.

A wide range of proteins are integrated into the skin's protective layer.

Punctate follicular porokeratosis is a skin condition with specific features seen in hair follicles.

A 69-year-old woman has a fast-growing hand lesion that didn't improve with salicylic acid.

Stem and progenitor cells in the eye have different division rates and locations, affecting how they respond to injury.

Skin lesions in Carney Complex are caused by a gene change in some skin cells that leads to increased pigmentation and may lead to tumors.

PEODDN is a rare skin disorder with limited treatment options, best treated with laser therapy.

A 15-year-old with KID syndrome developed a rare skin condition called PEHFN.

A new type of pachyonychia congenita linked to a specific keratin gene mutation was found in two Pakistani families.

Neutrophils quickly respond to skin injury.

Skin lesions in Carney complex are likely caused by a specific group of skin cells that promote pigment production due to a genetic mutation.

The upper hair follicle is stable, while the lower part allows movement during hair growth.

ZPK helps skin cells mature and may affect skin health.

Skin cells can naturally limit the growth of cancerous changes by balancing cell renewal and differentiation.

Ectopic acanthosis nigricans can occur at surgical sites due to skin graft mismatches.

The trichohyalin gene is located at chromosomal region 1q21 with other skin-related protein genes.

The man has a genetic skin condition called pachyonychia congenita.

Basement membrane changes in lichen planopilaris cause scarring and permanent hair loss.

A rare skin condition in a boy is likely due to a specific genetic mutation pattern.

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

Platelet-rich plasma therapy may rarely trigger herpes zoster ophthalmicus.