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Mice with too much sPLA₂-IIA have hair loss and poor wound healing due to abnormal hair growth and stem cell depletion.

HAIR-AN syndrome mainly affects obese women and can be improved with early diagnosis and treatment using insulin-sensitizing agents.

Girls with PCOS during adolescence have a higher risk of developing type 2 diabetes, and early treatment can help manage this risk.

A girl with a rare genetic condition affecting hair and nails also developed a common type of hair loss, suggesting a possible genetic link.

GAPO syndrome causes growth issues, hair loss, missing teeth, and vision problems.

K6hf is a unique protein found only in a specific layer of hair follicles.

Unique fat cells near fibrotic areas contribute to systemic sclerosis progression.

Type II keratin genes are crucial for hair follicle differentiation and have a conserved structure and expression pattern.

Pili annulati may be more common than thought, so recognizing its features is important for diagnosis.

A 9-year-old boy had a rare scalp condition usually seen in young men.

A woman's unique dementia was misdiagnosed, a genetic mutation increases Parkinson's risk with age, and finasteride may help with Tourette syndrome.

Two new mutations in the AR gene linked to severe androgen insensitivity were found.

Cells from a skin condition can create new hair follicles and similar growths in mice, and a specific treatment can reduce these effects.

Reduced alpha smooth muscle actin may cause hair loss in androgenetic alopecia.

Anorexia nervosa may cause a hair defect called pili torti due to malnutrition and high vitamin A levels.

A rare skin condition in a boy is likely due to a specific genetic mutation pattern.

A specific gene mutation in KRT86 is linked to hair disorder in a Chinese Han family.

Upadacitinib successfully regrew hair in a child with alopecia universalis and specific genetic mutations.

Hair loss may indicate higher risk of heart disease.

A 4-year-old boy has a rare type of hair loss in a line pattern on his scalp.

Four new cases of Bachmann-Bupp syndrome suggest potential for targeted treatment.

Adolescents with hair loss show different hormone levels by sex and often have related metabolic issues.

Mutations in the hHb6 gene cause the hair disorder monilethrix.

Abnormal contraction of connective tissue in hair follicles causes hair loss by killing off important cells, and treating this could improve hair growth.

A 21-year-old male with a rare genetic disorder experienced sudden hair loss and high DHEAS levels, likely due to a condition similar to PCOS, usually seen in women.

A virus protein can activate a pathway that may lead to abnormal hair follicle development.

ACKR2 helps prevent skin scarring and hair loss by controlling inflammation.

Alopecia areata is a type of hair loss that can lead to complete baldness, often associated with other autoimmune conditions, and half of the cases may see hair return within a year.

A new mutation, Glu402Lys, in hair keratin is linked to variable symptoms of monilethrix.

AKN might be a skin marker for metabolic syndrome.