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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 specific gene change plus an additional mutation in the same gene cause hereditary trichilemmal cysts.

A young woman had a rare scalp tumor usually found in older women.

Reduced CD44 expression may cause abnormal hyaluronate buildup in cutaneous myxoma.

Antibodies help identify glycoproteins in normal skin and tumor cells.

Mutations in the SHH pathway in certain skin cells can cause skin tumors and abnormal hair growth.

TSC2-/meth cells can cause skin lesions, hair growth, and lung issues, and may be treated with chromatin remodeling agents.

Mollugin may help treat diseases and boost hair growth and anti-aging.

Mice lacking a key DNA methylation enzyme in skin cells have a lower chance of activating stem cells necessary for hair growth, leading to progressive hair loss.

The first Japanese family with Marie Unna hereditary hypotrichosis showed hair condition improvement in a child and highlighted the risk of misdiagnosis.

Systemic mastocytosis may cause a type of hair loss called cicatricial alopecia.

Seborrheic keratosis is a common, harmless skin growth that can look like cancer, so it may need a biopsy.

Fatp4 is crucial for healthy skin development and function.

The study created a mouse model that survives longer and shows fewer symptoms of pemphigus vulgaris.

Increased cell death and reduced cell growth in hair follicles contribute to baldness.

Estrogen is important for keeping adult mouse nipple skin healthy by controlling certain cell signals.

EGFR deficiency in skin causes hair follicle issues and inflammation.

Drosha and Dicer are essential for hair follicle health and preventing DNA damage in skin cells.

Removing integrin α3β1 from hair stem cells lowers skin tumor growth by affecting CCN2 protein levels.

The keratin network in mouse skin changes during cornification and affects the skin's protective barrier.

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

A boy's skin fragility and sparse hair were caused by a genetic mutation affecting skin cell adhesion.

Adam10 enzyme is crucial for healthy skin and proper Notch signaling.

Two cows had a rare hair disorder causing hair loss but were otherwise healthy.

Certain mature cells in mouse lungs can turn back into stem cells to aid in tissue repair.

A 5-year-old girl has lipoid proteinosis, causing voice issues, hair thinning, skin lesions, and tongue movement problems.

Mature cells can re-enter the cell cycle and potentially lead to cancer.

Widened sweat ducts are a very specific sign of scarring hair loss.

People with Myotonic Dystrophy type 1 are more likely to have certain skin conditions, but not more likely to get skin cancer.