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Alopecia areata causes sudden hair loss, has genetic links, and can be managed but not cured.

Four genetic risk areas related to male-pattern baldness were identified, with WNT signaling playing a role in its development.

Male pattern hair loss is genetic and influenced by hormones, with treatments like minoxidil and surgery available.

Genetic data can predict male-pattern baldness with moderate accuracy, especially for early-onset cases in some European men.

Acne is significantly influenced by genetics, and understanding its genetic basis could lead to better, targeted treatments.

Genetic marker rs12558842 strongly linked to male hair loss.

Genetic research has advanced our understanding of skin diseases, but complex conditions require an integrative approach for deeper insight.

Alopecia areata, a type of hair loss, is likely an autoimmune disease with a genetic link, but its exact cause is still unknown.

The current understanding of frontal fibrosing alopecia involves immune, genetic, hormonal factors, and possibly environmental triggers, but more research is needed for effective treatments.

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

Genetic factors affect hair loss, and molecular testing may help predict, diagnose, and treat it.

Both genetics and lifestyle factors contribute to male pattern baldness.

Women with hirsutism have different levels of omentin-1, which may be linked to the condition and its genetic aspects.

A new mutation in the CYP11B1 gene was found in a woman with mild hyperandrogenemia, a rare cause of non-classic congenital adrenal hyperplasia.

A genetic test can identify people at risk of male pattern baldness early, allowing for quicker treatment.

Sphynx cats are hairless and Devon Rex cats have curly hair due to specific genetic mutations.

Certain genetic markers linked to reproductive potential were identified by their impact on a protein's ability to bind to genes.

Certain genetic variations in OCT1 may improve insulin sensitivity with metformin in women with PCOS.

Certain genetic variants are linked to frontal fibrosing alopecia in Spanish patients.

Certain genetic variants linked to immune response increase the risk of alopecia areata in Taiwanese people.

Hair loss is more common in male Chinese college freshmen, and it's linked with rosacea but doesn't affect their quality of life.

Combining genetic and physical trait analysis improves diagnosis accuracy for monogenic diabetes.

A genetic variant linked to hair thinning in Japanese women was found.

Nonclassic adrenal hyperplasia is a genetic condition that can cause early puberty and fertility problems, treated with specific steroids.

Nonclassic congenital adrenal hyperplasia is a genetic disorder causing hormone imbalances, affecting fertility and requiring personalized treatment.

The conclusion suggests that PCOS may persist due to genetic traits that, while harmful for female fertility, could have provided survival and reproductive benefits to males.

CAH is a genetic disorder affecting cortisol production and causing hormonal imbalances, with treatment and diagnosis varying by form and symptoms.

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

PCOS is a genetic disorder affecting women's reproductive health, with treatments focused on symptoms like insulin resistance and fertility.