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Researchers found a new gene area linked to male-pattern baldness, which, along with another gene, significantly increases the risk of hair loss in men.

Niacin derivatives may increase hair fullness in women with hair loss.

Two treatments for male pattern hair loss are minoxidil and finasteride, but they have side effects and may not satisfy everyone.

Female pattern hair loss involves hormonal factors, genetics, and may be linked to low ferritin levels.

Minoxidil can help thicken hair in some people with male pattern baldness, especially if used early and continuously.

Certain immune-related proteins are higher in people with alopecia and their healthy relatives, hinting at a genetic link.

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

A specific genetic marker is linked to male pattern baldness in Han Chinese men.

Male pattern baldness is an unintended side effect of the body's use of androgens for muscle growth, especially in those genetically prone to it.

Mutations in mitochondrial DNA might significantly contribute to the development of Polycystic Ovarian Syndrome.

Familial factors affect hair loss types in Koreans, with M type in men, L type in women, and paternal factors influencing male hair loss more.

Different women's hair and skin glands respond to hormones in varied ways, which can cause unwanted hair growth even with normal hormone levels, and more research is needed to treat this effectively.

Hormones and genetics play key roles in male and female baldness, which can affect mental health and may be linked to other health issues.

Midscalp hair density and terminal hair percentage are good indicators of female pattern hair loss severity.

Review determines effective, safe treatments for female hair loss.

Advancements in hair biology include new treatments and tools for hair growth and alopecia.

Hair loss in children is diagnosed and treated differently than in adults, with different common causes and a focus on less invasive methods.

The document concludes that primary scarring alopecias cause permanent hair loss, have unpredictable outcomes, and lack definitive treatments, requiring personalized care.

Blood tests can help understand the genetic differences in people with alopecia areata, including how severe it is and if it's inherited.

The baby’s hair loss was due to a rare genetic condition, not treatable by usual methods.

The report concludes that PCOS is mainly a condition of excess male hormones and its definition may change as new information is discovered.

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

Frontal Fibrosing Alopecia's cause is unclear, affects mainly postmenopausal women, and current treatments focus on stopping hair loss rather than regrowth.

Children's hairlines change shape as they grow, with women often developing a widow's peak and men's hairlines becoming more convex and possibly balding at the temples, influenced by genetics and hormones.

Two siblings both had a rare case of alopecia areata at the same time.

Two mouse mutations cause similar hair loss despite different skin changes.

There is no cure for myotonic dystrophy type 1, so treatment focuses on managing symptoms and complications.

Scientists have found specific genes linked to different hair loss conditions, which could lead to new treatments.

Men who start balding at age 20 may have a higher chance of getting aggressive prostate cancer.

Men with more severe hair loss had a lower risk of schizophrenia, but hair loss and testosterone levels were not linked.