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A woman with systemic sclerosis developed a unique scarring hair loss combining features of systemic sclerosis and frontal fibrosing alopecia.

A new mutation in the KRT86 gene was found to cause the hair disorder monilethrix in a Han family.

A protein made in a plant stopped hair growth in mice.

Two new gene mutations cause a rare hair disorder.

A 66-year-old man with a rare case of male frontal fibrosing alopecia did not regrow hair despite treatment.

A 66-year-old woman experienced hair loss due to Frontal Fibrosing Alopecia, a condition with no consistently effective treatment, but it usually stabilizes over time. More research is needed for better understanding and treatment options.

A new genetic disorder caused by an ODC1 mutation can be treated with DFMO.

A unique gene mutation was found in a family with monilethrix.

The patient has frontal fibrosing alopecia (FFA).

A new gene mutation causes vitamin D resistance and hair loss in two unrelated girls.

Certain defective glucocorticoid receptor mutants move faster inside cell nuclei and work less effectively.

Researchers successfully grew hair follicle stem cells from mice and humans, which could be useful for tissue engineering and regenerative medicine.

Two siblings have a rare hair condition caused by a new genetic variant.

Increased sunscreen use may be linked to frontal fibrosing alopecia in Hispanic females.

A woman with a unique syndrome similar to TRPS has a genetic change near the TRPS1 gene, affecting its regulation.

A mother and daughter with similar hair loss conditions and identical HLA types suggest a genetic link between the conditions.

A mutation in the iRhom2 gene causes hairless mice due to abnormal hair follicle development.

Dermoscopy helps diagnose frontal fibrosing alopecia by distinguishing it from other hair loss conditions.

Hereditary elliptocytosis causes elongated red blood cells and can lead to mild or no symptoms.

Certain gene variations may increase the risk and severity of alopecia areata.

Frontal Fibrosing Alopecia is a slowly progressing hair loss condition, likely underdiagnosed, with ineffective treatments, needing more research to understand it fully.

Ferrous Ferric Chloride may improve skin cell function and increase hair growth in mice.

FGF-1 causes spiral ganglion neurites to branch more.

Er:YAG laser therapy effectively treats Hailey-Hailey disease, leading to long-term remission and improved quality of life.

Mutations in the KRT85 gene cause hair and nail problems.

Frontal fibrosing alopecia can cause sudden hair loss on limbs, similar to scalp hair loss.

New SRD5A2 variants may disrupt protein function, aiding diagnosis and treatment of related disorders.

TCF/Lef1 activity is essential for proper skin cell development and renewal.