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Some children who had stem cell transplants developed permanent hair loss, especially when treated with a drug called busulphan.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

Certain fats in the blood are linked to an increased risk of male pattern baldness.

Certain genetic mutations can lower bad cholesterol and reduce heart disease risk, leading to effective cholesterol-lowering drugs.

Androgens can help prevent memory problems caused by apoE4.

Most patients with Porphyria Cutanea Tarda had skin blisters and were often affected by hepatitis C and alcohol abuse, with differences between familial and sporadic cases.

Hepatitis B virus exposure may be linked to increased risk of alopecia areata.

A specific gene variant causes severe skin issues and increases infection risk, requiring careful medical monitoring.

A complex X chromosome rearrangement can increase the risk of multiple autoimmune diseases.

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

Shorter telomeres in white blood cells may increase the risk of a common type of hair loss.

Vitamin D helps protect skin, PSORS1 gene's risk interval for psoriasis is expanded, hair follicles can be generated from mouse cells, and interferon-γ may cause pigmented skin lesions.

The study found that alopecia areata and hypothyroidism increase the risk of each other, but androgenetic alopecia and hypothyroidism do not.

PCOS is often caused by hormonal imbalances that can lead to various health issues and may indicate a risk for future metabolic and cardiovascular problems.

Genetic variations greatly affect individual metabolism and can impact health and disease risk.

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

The tumor suppressor gene FLCN affects mitochondrial function and energy use in cells.

Certain SHBG gene variants, like rs727428, are linked to higher testosterone levels in women with PCOS.

Topical minoxidil helps treat female pattern hair loss, but more research needed for other treatments.

Researchers found two new genetic variants linked to Alzheimer's disease.

Men with less sun-sensitive skin have lower PSA levels, while men with more sun-sensitive skin have higher PSA levels.

Long-term high testosterone levels can improve bone density and reduce body fat but may increase the risk of prostate cancer and high blood pressure.

Some people have a genetic variation that makes them less effective at breaking down drugs.

Certain surgical methods are better than routine incision for hidradenitis suppurativa, topical clindamycin and acitretin are effective treatments, men with HS have a risk of skin cancer, HS patients are more likely to die from heart problems, and specific genetic markers are linked to treatment response.

Diet changes can protect against harmful environmental effects on fetal development.

Shorter CAG repeats may cause hair and skin issues, while longer ones may link to acne.

The environment around the time of conception can change the VTRNA2-1 gene in a way that lasts for years and may affect disease risk.

The document suggests treating individuals with nonclassic congenital adrenal hyperplasia who show symptoms, especially those related to excess male hormones.

ESR2 gene variations may be linked to female pattern hair loss.

Alopecia areata causes hair loss due to an immune attack on hair follicles, influenced by genetics and environment.