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The review found no clear link between vitamin D receptor gene variations and polycystic ovary syndrome.

Men with more vanadium in their blood and who drink less soy milk are more likely to have hair loss.

Four genetic risk spots found for hair loss, with WNT signaling involved and a link to curly hair.

Boys with less severe EDA mutations in XLHED have milder symptoms and better sweat and hair production.

Certain skin conditions may indicate or increase the risk of Parkinson's disease.

Certain gene variations increase the risk of alopecia areata in Koreans.

Hyperandrogenism increases heart disease risk in premenopausal women, but this risk is linked to obesity in postmenopausal women.

A certain genetic variation in the IL1A gene may lower the risk of a hair loss condition in Chinese people.

A genetic variant in the androgen receptor gene increases heart disease risk in women but not in men.

Most children with a common hemochromatosis genotype had elevated iron levels but no severe symptoms.

Both genes and environmental factors like chemicals may contribute to the increase in hypospadias, but the exact causes are still unclear.

People with hypohidrotic ectodermal dysplasia are more likely to experience long-term fatigue and hair loss after COVID-19.

Finasteride dosages should be adjusted based on CYP3A5 genotype and liver function to avoid side effects.

Certain gene variations may increase the risk of alopecia, and platelet-rich plasma treatment can improve hair density in those with hair loss; a rare case of facial Becker's nevus was linked to uneven beard growth.

Low testosterone in men is a risk factor for a specific heart rhythm issue, and testosterone treatment may help prevent it.

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

ADT, especially enzalutamide, may increase the risk of heart rhythm problems and sudden death in men.

Human enzymes can detoxify harmful substances but might also increase their cancer risk.

Oral contraceptives lower testosterone levels in women, especially those with certain genetic traits, and may be linked to increased breast cancer risk.

Low birthweight and rapid weight gain after birth may increase the risk of developing polycystic ovary syndrome.

Certain gene variations in EGF and EGFR may increase the risk of alopecia areata in Koreans.

Higher levels of β-carotene and vitamin E may help prevent certain types of hair loss.

5α reductase type 2 enzyme mutation and oxidative stress may increase androgenetic alopecia risk in Egyptians.

Androgens may influence T cells, contributing to higher autoimmune liver disease risk in women.

Certain gut bacteria may protect against alopecia areata, while others may increase the risk.

The first Japanese family with Marie Unna hereditary hypotrichosis showed hair condition improvement in a child and highlighted the risk of misdiagnosis.

Estrogen-progestin contraception lowers ovarian, endometrial, and colon cancer risk but may raise breast and cervical cancer risk, helps with menstrual and acne issues, and new methods are as effective as pills. Metformin helps overweight women with PCOS and insulin resistance, and dopamine agonists treat prolactinomas.

Toxic epidermal necrolysis is a severe skin condition often caused by drugs, with complex treatment and a high risk of death, but survivors usually heal without scars.

Non-classic congenital adrenal hyperplasia is a common disorder causing symptoms like acne and infertility, and it's managed based on symptoms, not just test results. Treatment can improve fertility and reduce miscarriage risk.

Pets in Egypt can pass skin fungus, especially Microsporum canis, to humans, with outdoor and young pets being more at risk.