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Nestin marks cells that can become a specific type of skin cell in hair follicles of both developing and adult mice.

Lysocellin helps stop cell damage from etoposide and may prevent hair loss.

A child's rare skin disease was triggered by chickenpox.

Lichen planopilaris is more common in older women and may be linked to hormone therapy and autoimmune diseases.

A girl with no hair neglect developed plica neuropathica in the hospital, lost all her hair, but it grew back.

Proper niche formation in Drosophila requires Slit-Robo signaling for cell migration.

The piglets fully recovered from psoroptic mange after treatment.

An 8-year-old girl has a rare, irreversible hair loss condition caused by a genetic mutation.

A 2-year-old girl had a hair disorder not shared by her identical twin.

Topical minoxidil may help treat a rare genetic hair condition with no fully effective treatments yet.

Specific immune cells and pathways contribute to hair follicle inflammation and hair loss, suggesting potential treatments for lichen planopilaris.

A pilomatrixoma in the eyebrow can cause hair loss and skin lightening.

Contact immunotherapy helped hair regrow in a patient with both alopecia and psoriasis.

Hair loss can occur when pemphigus foliaceus changes to pemphigus vulgaris.

A PKP1 gene mutation causes skin fragility and hair loss in Chesapeake Bay retriever puppies.

A new gene mutation caused a man's rare skin condition, Schöpf-Schulz-Passarge syndrome.

Platycladus orientalis leaf extract helps hair grow by activating certain proteins.

Netherton's disease causes multiple hair defects.

PCOS often causes skin problems due to hormonal and metabolic imbalances.

The study found unique skin changes in a rare type of alopecia linked to a skin condition called linear morphea.

Lizards can regrow their tail scales with the same structure, distribution, and gender-specific features as the original ones, and this unique ability is not seen in adult mammals.

A rare skin reaction from cancer treatment was successfully managed with topical treatments and antihistamines.

Understanding the genetics of rare inherited ichthyosis syndromes is key for better treatments and genetic counseling.

Keratin mutations may cause scarring alopecia by damaging hair structure.

The enzyme DHHC13 is essential for healthy hair and skin, and its deficiency leads to hair loss and skin problems.

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

Scalp edema may be a new variant of conditions reacting to scarring alopecia like LPP.