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A 73-year-old woman with Hypopigmented Mycosis Fungoides, a rare skin lymphoma, experienced disease progression despite treatment, emphasizing the need for ongoing monitoring.

Trichoscopy can help diagnose and decide when to biopsy folliculotropic mycosis fungoides.

FGF13 gene changes cause excessive hair growth in a rare condition.

A person got uncombable hair syndrome from two copies of chromosome 1 from their mother.

Hutchinson-Gilford Progeria Syndrome causes rapid aging from a genetic mutation, with no cure but ongoing research into potential treatments.

The mutant HR bmh protein mis-localizes in cells, affecting skin and hair development.

A new mutation in the CDH3 gene causes hair loss and vision problems in a young girl.

Hair follicle sampling is a practical method for measuring biomarkers in children with and without Fragile X syndrome.

Frontal fibrosing alopecia in families shows similar signs to individual cases and may have a genetic link.

Dermoscopy helps diagnose folliculotropic mycosis fungoides by identifying specific skin patterns.

Frontal fibrosing alopecia is a scarring hair loss condition mainly affecting older women, with no known cause and treatments that may help stabilize hair loss.

Researchers found a new way to create hair-growing structures in the lab that can grow hair when put into mice.

FGF5 gene mutations cause long hair in domestic cats.

Hepatitis C treatment may cause frontal fibrosing alopecia.

A new mutation in the HR gene is linked to a rare form of hair loss with limb deformities.

Researchers found an RNA transcript that might help control a growth factor linked to tumor development.

FFA in young women is often missed, and no single treatment works best.

The flaky skin mouse mutation is a natural model for studying human psoriasis.

Early diagnosis and treatment are crucial for managing Folliculotropic Mycosis Fungoides on the scalp.

Follicular mycosis fungoides can look like a B-cell lymphoma, making diagnosis difficult.

Different forms of FGF5 either promote or inhibit hair growth.

Four new FGF5 gene variants cause long hair in dogs.

FFA in men, often mistaken for other hair loss types, may be more common than thought and needs larger studies for confirmation.

The modified Ferriman-Gallwey method is a useful tool for diagnosing hirsutism.

Hoyeraal-Hreidarsson syndrome in infants causes severe gastrointestinal issues.

A new mouse hair mutation, called hague, is semidominant and unstable, but the exact cause is unknown.

Dermoscopy helps diagnose frontal fibrosing alopecia by identifying specific scalp features.