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Genetic variants can affect valproic acid's effectiveness, side effects, and levels in epilepsy treatment.

Afro-textured hair needs personalized care due to its unique genetic traits.

Doctors should consider Netherton syndrome in patients with chronic skin and hair issues to avoid misdiagnosis.

Early-onset baldness is linked to genetics, lifestyle, and can indicate higher risk for heart and metabolic diseases, and affects mental health.

Genetic research may lead to better ways to predict and treat male-pattern hair loss.

The study suggests that hypothyroidism may cause alopecia areata.

Immune cells are essential for early hair and skin development and healing.

Rare genetic variants in five specific genes are linked to male-pattern hair loss but only account for a small part of the risk.

Seborrheic dermatitis may contribute to the development of central centrifugal cicatricial alopecia.

Alopecia areata is complex, often recurring, and needs personalized treatment, especially with other health issues.

Hairlessness in mammals is due to complex genetic changes in both genes and regulatory regions.

Certain genetic changes in the LSS gene cause a rare skin and hair condition.

New genetic mutations linked to rare skin disorders were found in three newborns.

The genetic variant studied does not affect PCOS symptoms in Kashmiri women.

Certain genetic markers can indicate higher or lower risk for systemic lupus erythematosus.

The girl's unexpected pubic hair growth led to a diagnosis different from complete androgen insensitivity syndrome.

A genetic mutation in the EDA gene causes hypohidrotic ectodermal dysplasia in cats.

Genes controlling hair growth and immune response are disrupted in male pattern baldness.

The study found that genetic differences related to hair growth and other traits help cashmere goats adapt to high-altitude environments.

A specific genetic change is linked to mental disorders, intellectual disability, and possibly autoimmune disease in a family.

A specific genetic marker is linked to male pattern baldness in Han Chinese men.

A cat's poor wound healing was linked to a genetic deletion in the COL5A1 gene.

Tandem repeats significantly influence hair color, especially darker shades, across different ancestries.

Fibrodysplasia ossificans progressiva is a rare genetic disorder that causes extra bone growth and symptoms of premature aging.

Thiopurines help treat IBD but require genetic testing to avoid side effects.

A new gene variant causes glucocorticoid resistance in a mother and son.

Three siblings with a rare genetic condition had abnormal sexual development and chose different gender identities, needing surgery and therapy.

Fingerprints form uniquely before birth due to specific genetic pathways and local signals.

New treatments are needed for PCOS that target its genetic, hormonal, and metabolic causes.

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