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Hormonal imbalances can cause skin and hair problems in women, and treatments that block male hormones can help.

Pattern baldness is likely caused by a dominant gene influenced by testosterone levels, making it more common in men.

A patient developed hair loss after hepatitis C treatment with sofosbuvir and ribavirin.

There's no significant link between hair loss from male pattern baldness and early heart disease.

Bald men may have a higher risk of heart disease, but baldness doesn't necessarily mean more severe heart disease.

Alopecia Areata is linked to a higher risk of several diseases, which vary with age and sex.

Men's and women's pattern hair loss progress differently, with men showing more hair thinning and women having more widespread hair loss.

Excessive sun protection might cause frontal fibrosing alopecia by disrupting skin immune balance.

A woman lost all her body hair after hepatitis C treatment, but it started to grow back a year after stopping the treatment.

Coloring shampoos for gray hair may cause gene mutation, reproductive issues, and skin damage, needing stricter regulation and expert consultation.

Long-term use of finasteride and dutasteride can cause serious health issues like diabetes and liver problems.

SARMs may be an effective treatment for a certain type of breast cancer by blocking cancer growth and spread.

Recognizing LET and AITD can help diagnose SLE early for better treatment.

A man had a rare skin cancer that looked like a bald spot.

The rs6152 allele is not a good marker for baldness in the Indonesian population, but family history, age, gender, high blood pressure, and body weight are linked to the risk.

Rare genetic variants in 125 genes are linked to male-pattern hair loss.

Cholesterol sulfate buildup due to a genetic mutation disrupts the skin barrier, leading to the scaling skin seen in X-linked ichthyosis.

Thiopurines help treat IBD but require genetic testing to avoid side effects.

Testosterone is linked to cardiovascular risk factors and stroke, but its exact role is unclear.

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

Genetic variation in the androgen receptor gene mainly causes early-onset hair loss, with maternal inheritance playing a key role.

Hormones and their receptors, especially androgens, play a key role in hair growth and disorders like baldness.

A new mutation in the STING protein causes a range of symptoms and its severity may be affected by other genetic variations; treatment with a specific inhibitor showed improvement in one patient.

Adding Triamcinolone to the anesthetic can reduce swelling after hair transplants, and using Platelet-Rich Plasma can improve hair thickness and patient satisfaction. The SRD5A2 gene also plays a key role in the success of hair transplants.

Cytochrome P-450 enzymes in the skin help break down various substances and could be targeted to treat skin conditions.

Family history, especially on the mother's side, increases the risk of female pattern hair loss.

The skin's bacteria might influence the development of a hair loss condition called alopecia areata.

Iron deficiency is a common nutritional cause of hair loss.

Msx2 and Foxn1 are both crucial for hair growth and health.

The document concludes that the androgen receptor's structure and function are complex, affecting how it regulates genes and is involved in diseases like prostate cancer.