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New treatments for skin conditions related to the sebaceous gland are being developed based on current research.

Platelet-rich plasma may help hair follicle cells grow by affecting certain genes and pathways.

Women with AGA have higher lipid levels, increasing heart disease risk.

Childhood ptosis can vary from a minor cosmetic issue to a serious condition and may signal other health problems.

The document concludes that hormonal biomarkers are key for diagnosing hyperandrogenemia in women and hypogonadism in men.

Acne is caused by multiple factors including oil production, bacteria, inflammation, and possibly diet and environment.

The severity of symptoms in nonclassical congenital adrenal hyperplasia is not determined by CYP21A2 gene variations.

Sex hormones, especially estradiol, can change chicken feather shapes and colors.

A gene mutation causes woolly hair in a Syrian patient.

No clear link between androgen receptor variation and hair loss, but more research needed.

The PP2A-B55α protein is essential for brain and skin development in embryos.

Testosterone significantly affects sexual desire in both men and women, but its impact on women is more complex and influenced by psychological factors.

DNA phenotyping helps predict physical traits from DNA with varying accuracy and requires careful ethical and legal handling.

New ABCA12 gene mutations were linked to a skin condition with scaling and hair loss, and a treatment helped with hair loss in a related case.

The main enzyme found in pubic skin that could be targeted to treat excessive hair growth is 5 alpha-R2.

A mutation in the FAM83G gene is linked to skin and hair abnormalities in two related individuals.

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

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

The document concludes that managing female hyperandrogenism requires a combination of identifying the cause, lifestyle changes, medication, and cosmetic treatments.

Changes in the HR gene have influenced hair growth and may lead to hair loss conditions in humans.

Mutation in hairless gene may increase hair loss risk.

The AIRE gene variant rs2075876 is linked to a higher risk of alopecia areata in males.

Key genes linked to hair growth and cancer were identified in hairless mice.

Using SNP array testing helped quickly find the gene causing Woodhouse-Sakati syndrome in two related individuals.

The we/we wal/wal mice have defects in hair growth and skin layer formation, causing hair loss, useful for understanding alopecia.

Over half of the children had abnormal hair under a microscope, with many having genetic hair conditions.

The study concluded that a protein important for hair strength is regulated by certain molecular processes and is affected by growth phases.

Dermal EZH2 controls skin cell development and hair growth in mice.

Blocking DGAT1 reduces oil gland size in mice and dogs, but only mice experience hair loss.

Pig skin cells can turn into mesodermal cells but lose their ability to become neural cells.