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Skin organoids with NCSTN mutation show changes in hair follicle development and higher inflammation, key features of Hidradenitis Suppurativa.

Skin problems after waxing led to a sarcoidosis diagnosis.

ODC transgenic mice can model human hair loss with skin lesions.

A rabbit gene important for hair development was identified and detailed.

The girl's skin condition is benign but challenging to treat due to its size and location.

A 6-year-old girl with Turner syndrome also had psoriasis, alopecia areata, and trachyonychia.

Calcifying epithelioma cells can differentiate into hair cortex and outer root sheath.

Short-term treatment with ROCKi increases skin cell growth without changing stem cell features.

Congenital atrichia with papular lesions causes permanent hair loss and skin bumps from birth.

A KRT32 gene variant causes loose anagen hair syndrome.

Trichoscopy helps accurately diagnose Netherton syndrome, often mistaken for atopic dermatitis.

Krtap11-1 is important for hair strength and structure.

Combining skin tissue pathology with genetics has greatly improved the diagnosis and understanding of certain skin diseases.

The young woman has a benign, hereditary skin condition with no signs of a more serious syndrome.

Mutations in the desmoplakin gene can cause hair problems and deadly heart disease.

A new genetic change in the DSC3 gene is linked to a rare condition causing hair loss and skin blisters in a child.

Keratin biomaterials from human hair help nerve regeneration by activating Schwann cells.

Trichoscopy is a helpful tool for diagnosing Netherton syndrome.

Hair follicle development involves specific cells and genes, crucial for understanding severe skin diseases like harlequin ichthyosis.

Half-siblings with a rare skin condition improved with treatment for a fungal infection, but hair loss remained.

A rare hair follicle tumor in the hand was successfully removed with no return after four years.

A boy and his father with hereditary hypotrichosis simplex were treated for hair loss, but the treatment result is unknown.

Genetic discoveries are key for understanding, diagnosing, and treating inherited hair and nail disorders.

ErbB2 signaling is crucial for skin cell growth and cancer development in mice.

Facial trichostasis spinulosa is a chronic condition with significant cosmetic impact, especially in young women.

Wnt/β-catenin signaling is important for keeping skin cell attachment structures stable.

Hair matrix cysts are rare skin nodules with unique features, often needing surgical removal.

A kidney transplant patient developed pink skin bumps with spiny centers on her face and limbs.

Keratin 15 affects cell behavior and characteristics in skin cells.