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A gene variant increases the risk of a type of hair loss by affecting hair protein production.

A new gene mutation linked to a skin condition was found in a Spanish family.

Early-onset baldness is linked to a higher risk of aggressive prostate cancer in African-American men, especially before age 60.

A certain gene variation is linked to a higher risk of polycystic ovarian syndrome in South Indian women.

Higher miR-34a levels and the A variant of the MIR-34A gene are linked to increased risk and severity of alopecia areata.

Certain genetic variants in the androgen receptor are linked to higher PSA levels, potentially affecting prostate cancer screening outcomes.

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

Patient-reported outcomes better reflect the quality of life impact of alopecia areata than traditional severity scores.

Certain gene variations and different levels of BDNF and CRH hormones are linked to vitiligo.

The review concludes that more research is needed to better improve the health outcomes for people with Polycystic Ovarian Syndrome.

Women with nonclassic congenital adrenal hyperplasia experience more sexual dysfunction and distress.

No consistent link between genotype and phenotype in 5-α-Reductase type 2 deficiency.

Swedish men with the E213 A-allele of the androgen receptor have a lower risk of prostate cancer.

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

The visfatin GT genotype may increase the risk of Alopecia Areata.

The C-allele and CC-genotype in the PTPN22 gene lower the risk of alopecia areata.

The IRS-2 Asp/Asp genotype may increase the risk of PCOS in Chinese women, especially if they are not obese.

The AIRE gene variant rs2075876 is linked to a higher risk of alopecia areata in males.

A certain genetic variation is linked to a higher risk of polycystic ovarian syndrome.

Certain genetic variants increase the risk of resistance to hormone therapy in prostate cancer patients.

Certain genetic variations in IL-16 may increase the risk of alopecia areata.

High levels of testosterone and anti-Müllerian hormone before pregnancy are linked to a higher risk of newborns needing intensive care.

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

The article concludes that global standardization in PCOS research is crucial for accurate diagnosis and understanding of the condition.

Siblings with signs of virilization should be tested for non-classical congenital adrenal hyperplasia, which does not affect adult height but may impact fertility and well-being if untreated.

A certain mutation in the fetal alpha 5-reductase gene is linked to a higher risk of late miscarriage.

Certain genes on chromosomes 6, 10, 16, and 18 may increase the risk of alopecia areata.

The meeting highlighted the genetic basis of female pattern hair loss and various skin health insights.

Some parents have a mild form of congenital adrenal hyperplasia without symptoms, and they usually don't need treatment.