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Men with early hair loss may have a higher risk of enlarged prostate and possibly prostate cancer due to shared hormonal factors.

Many adult women experience unexplained excessive hair shedding, often starting before age 40.

About 30% of women feel they lose too much hair, often starting before age 40, and most can't find a reason for it.

The exam tested knowledge on various skin-related topics for CME credit.

Many men with male pattern baldness have abnormal blood fat levels, which may raise their risk of heart disease.

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

Hormonal differences affect male pattern baldness.

Vitamin D and its receptor regulate skin functions like cell growth, immunity, hair cycle, and tumor prevention.

A new gene mutation causes female pseudohermaphroditism due to glucocorticoid resistance.

TNF family proteins are crucial for the development of skin features like hair, teeth, and mammary glands.

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

Understanding the genetics of rare inherited ichthyosis syndromes is key for better treatments and genetic counseling.

Tumor suppressors help control inflammation in cancer and restoring their function could lead to new treatments.

Genetic discoveries are key for understanding, diagnosing, and treating inherited hair and nail disorders.

Sebaceous glands are involved in various skin disorders, some treatable with medications like finasteride and minoxidil.

New and known mutations in the hairless gene cause a hair loss condition called Atrichia with papular lesions.

A mutation in the HR gene causes a rare form of irreversible hair loss in two Kashmiri families. Whole exome sequencing is effective for finding such mutations.

A baby from an Indian family had a rare genetic disorder causing no scalp or body hair due to a specific gene deletion.

Uncombable hair syndrome causes frizzy hair and can affect the nervous system, eyes, and ears, often co-occurring with other hair, skin, nail, and teeth conditions, and is linked to three specific gene mutations.

The document concludes that an experimental drug may help wound healing in Epidermolysis Bullosa, links Hydroa vacciniforme to EBV, discusses diagnosing hair loss disorders, finds many children with eczema have allergies, reviews the safety of a skin medication in children, notes side effects of a Duchenne's treatment, and identifies a marker for pediatric mastocytosis.

The document concludes that Borrelia afzelii causes a skin condition in France, a gene is linked to hair loss in Caucasian women, and various genetic mutations affect skin diseases.

Vitiligo is a skin condition causing white spots, more common in women, often starts before age 20, and can affect mental health.

The research found that PCOS has common genetic factors regardless of how it is diagnosed and is linked to metabolic and reproductive issues.

The conclusion is that using drugs to block the TOR pathway might slow aging and prevent age-related diseases.

Hidradenitis suppurativa, a chronic skin disease, can be managed with antibiotics, lifestyle changes, and in severe cases, surgery. Early diagnosis and careful planning are key, and laser treatment can be an efficient solution for mild to severe cases.

Msx and Dlx genes are crucial for development, controlling cell behaviors like growth and differentiation through their roles as gene regulators.

Visible light can damage skin and most sunscreens don't block it well; more research is needed on its effects and protection methods.

Hair loss needs more research for better treatments.

AGA more common in men, Koreans have lower rates and unique patterns.

Male pattern baldness involves genetics, hormones, and needs better treatments.