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Polycystic Ovary Syndrome should be seen mainly as a condition of excess male hormones, with a focus on this in its definition.

Linagliptin slows down premature aging in certain mice.

The research found genetic differences in identical twins that could explain why one twin has a disease while the other does not.

A new gene mutation causes insulin resistance in a girl and her mother.

Sex hormones affect hair and feather growth and may help manage alopecia and hormone-dependent cancers.

DFMO treatment improves hair growth, muscle tone, and development in Bachmann-Bupp syndrome patients.

The TRPV3 gene variant may cause the long-haired suri alpaca coat.

Patients with certain FoxN1 gene mutations have severe immune issues but normal skin and hair.

A specific thyroid hormone resistance mutation may be linked to different types of hair loss.

Hair follicle stem cells are controlled by their surrounding environment.

Kids with early graying hair often have low levels of calcium, ferritin, and vitamin D3.

Sebum from sebocytes is important for skin health and linked to conditions like acne and hair loss.

Polycystic ovary syndrome (PCOS) is more common in urban areas, possibly due to lifestyle and diet, and ignoring it can lead to serious health issues.

Loss of Msx2 function causes eye development issues similar to Peters anomaly.

Schizophrenia risk genes may affect early brain development, contributing to the disease.

The Gsdma3 gene is essential for normal hair development in mice.

High triglyceride levels are a key factor affecting testosterone levels in women with PCOS.

The vitamin D receptor can work without its usual activating molecule.

Impaired androgen production in 46,XY DSDs causes ambiguous genitalia and requires long-term care.

A girl with Becker naevus syndrome has a genetic variant in the ACTB gene related to her symptoms.

Blond hair in Solomon Islanders is due to a unique genetic variant, not European ancestry.

Some brain cancer cells avoid immune system detection, and certain treatments could target this to slow their growth; also, certain fat cell precursors help regenerate hair and skin after injury.

New genes linked to ichthyosis were found, but there's still no cure; treatment options are improving.

Certain genetic markers, especially the MICA gene, are linked to alopecia areata.

Mutations in the WNT10A gene can cause skin, hair, teeth, and other disorders, and may also affect other areas like kidney and cancer, with potential for targeted treatments.

KRT14 gene variants cause dermatopathia pigmentosa reticularis, affecting nails, teeth, and hair.

There's no significant genetic link between male pattern baldness and COVID-19.

Researchers identified genes in scalp hair follicles that may affect hair traits and hair loss.

Deleting the MAD2L1 gene in mice led to rapid tumor growth despite chromosomal instability.

Basonuclin 1 (BNC1) helps skin cells multiply and move, which is crucial for wound healing.