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A genetic duplication on chromosome 5 was linked to a woman's unique combination of medical conditions.

Certain changes in the SHBG gene may increase the risk of PCOS in Iraqi women.

SNP rs2479106 in the DENND1A gene may increase PCOS risk in Saudi Arabian females.

The number of CAG repeats in the androgen receptor gene doesn't significantly affect female pattern hair loss in the Han Chinese population.

The human type II 5α-reductase gene has a specific structure important for understanding certain medical conditions.

Oral contraceptive use may increase the risk of frontal fibrosing alopecia in women with a specific CYP1B1 gene variant.

A new genetic variant in the EEF2K gene may contribute to polycystic ovary syndrome.

Targeting the TNFRSF1B gene may help treat hair loss.

Researchers found a new genetic mutation linked to a hair condition in a Japanese boy.

H1 increases risk for neurodegenerative diseases, while H2 offers protection but is linked to other disorders.

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

Certain genetic variations in IGF2BP2 and IGFBP3 are linked to a higher risk of PCOS.

TCDD speeds up skin barrier formation by increasing certain gene expressions.

Higher IL-37 levels are linked to more severe alopecia areata, but the gene variation doesn't affect disease risk.

Researchers found a specific immune receptor in patients that causes severe skin reactions to a drug.

Patients with the same vitamin D receptor mutation showed different symptoms due to other factors.

A position effect on the TRPS1 gene causes excessive hair growth in humans and mice.

PTEN was identified as a specific marker for the skin disease cutaneous lupus erythematosus, and it helps increase the expression of harmful type I interferons.

The Itpr3 gene causes a specific hair pattern in mice.

G allele of AR Stul polymorphism linked to higher hair loss risk, especially in white people.

Mutations in the SRD5A3 gene cause a new type of glycosylation disorder by blocking the production of a molecule necessary for protein glycosylation.

A new gene mutation is linked to monilethrix in the studied family.

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

CYLD mutations cause a variety of skin tumors with symptoms starting around age 16, and treatments are currently limited.

A new mutation in the TRPS1 gene was found in a Ukrainian girl with Trichorhinophalangeal syndrome type I.

A new mutation in the LIPH gene was found to cause a rare hair disorder in a Japanese boy.

Dual TCR Treg cells are common in mouse tissues and vary by location.

The FTO gene hinders stem cells in hair follicles from becoming pigment cells.