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The study found that a specific genetic variation in the TNFα gene is significantly linked to Alopecia Areata in the Jordanian Arab population.

Frontal fibrosing alopecia is linked to four genetic areas, especially the HLA-B*07:02 allele.

Certain genes may be linked to autoimmune conditions in people with alopecia areata.

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

Targeting IL-15 may help treat Alopecia Areata.

A gene mutation causes lanceolate hair in rats by disrupting hair shaft integrity.

A new genetic variant in the LIPH gene causes hair growth issues in a Chinese patient.

Hairless protein affects hair follicle structure by regulating the Dlx3 gene.

A new gene mutation causes vitamin D resistance and rickets, treatable with calcium therapy.

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

A girl had rickets due to a gene mutation affecting vitamin D response.

A new mutation in the Hr gene causes hair loss in mice, similar to a human hair disorder.

This enzyme helps metabolize fatty acids and isoleucine, and could be key in treating neurological diseases and certain cancers.

Malondialdehyde-modified DNA may trigger an immune response in alopecia areata patients.

A gene variant causes patched hair loss in mice, similar to alopecia areata in humans.

Genetic testing for hairless gene mutations is crucial to correctly diagnose and treat atrichia with papular lesions.

Genetic variants at 20p11 increase baldness risk in Chinese Han people.

A new EDA gene variant causes X-linked hypohidrotic ectodermal dysplasia in a Chinese family.

The rs231775 genetic variant is linked to a higher risk and severity of Alopecia Areata in males.

The hairless (hr) gene is essential for normal hair follicle function and its mutation leads to hair loss.

The gene for Marie Unna hereditary hypotrichosis is located on chromosome 8p21, near the hairless gene.

EDA2R gene linked to hair loss.

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

Four genes are linked to alopecia areata, with two increasing risk and two offering protection.

Higher levels of certain DNAs in blood may indicate hair follicle damage in alopecia areata patients.

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

PRDX5 enzyme may contribute to alopecia areata by affecting oxidative stress and autoimmunity.

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

Certain IL-18 gene variations may increase the risk of alopecia areata.