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

A specific mutation in the K25 gene causes a rare genetic disorder with curly hair at birth and later hair loss, along with dental issues.

Stem cells are crucial for wound healing and understanding their role could lead to new treatments, but more research is needed to answer unresolved questions.

Polycystic Ovary Syndrome (PCOS) was found in 3.86% of tenth-grade girls in Guangzhou, China, with higher rates in overweight and obese girls, suggesting diagnosis should focus on hyperandrogenemia.

Melanocytes are important for normal body functions and have potential uses in regenerative medicine and disease treatment.

Hair keratin-associated proteins are essential for strong hair, with over 80 genes showing specific patterns and variations among people.

Patients with severe alopecia areata have higher levels of MIF, which decrease after successful treatment.

Targeting androgen receptors could be a promising way to treat skin disorders with fewer side effects.

Different harmful mutations in the CDH3 gene cause HJMD, but symptoms vary among individuals.

Women with early hair loss have higher blood pressure and aldosterone; screening and treatment may help.

Accurate clinical, histological, and genetic methods are key for understanding and treating hair disorders.

Dehydroepiandrosterone (DHEA) is a prohormone important for producing sex steroids and has potential health benefits.

Some skin conditions may indicate metabolic syndrome, which could help with early detection and management of related health issues.

Hormonal treatments can improve acne, but they come with potential side effects and risks.

High levels of male hormones in pregnant mice cause heart enlargement and poor heart function in their female babies.

Hair follicle stem cells help skin heal and grow during stretching.

Liraglutide caused significant weight loss in some obese women with PCOS, especially those with severe obesity and insulin resistance.

Most Hairless gene mutations reduce its ability to work with the Vitamin D Receptor, which might explain a certain type of hair loss.

Finasteride irreversibly affects human steroid 5α-reductase 2, providing insight into its catalytic mechanism and disease-related mutations.

High levels of TNF-α may contribute to obesity and insulin resistance in PCOS, but not due to the C850T genetic variation.

Mice lacking steroid 5α-reductase 2 show less aggression and better impulse control.

Women with nonclassic 21-hydroxylase deficiency can have successful pregnancies through IVF, with certain factors affecting their chances.

Young HS patients often have other physical and mental health issues, and research on HS covers a wide range of topics including genetics, triggers, treatments, and the need for more data.

The review suggests a comprehensive approach to treat hirsutism, focusing on hair removal, medication, and managing emotional effects.

Effective acne management in PCOS includes hormone therapy, metformin, isotretinoin, weight loss, diet, exercise, and personalized treatment plans.

Certain Prakruti types are more prone to early male pattern baldness.

Nails can reveal important health information about skin and body conditions.

A group has developed therapies that show promise for treating cancer and various other conditions.

Women with the NIH type of PCOS have more obesity and higher risk of diabetes and heart disease than those with other types of PCOS.

Exposure to too much androgen before birth might cause polycystic ovary syndrome later in life.