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The new method found new shared genetic areas linked to both Type 2 Diabetes and Prostate Cancer.

Researchers found a new area on chromosome 2 linked to a genetic hair loss condition.

A rare autoimmune condition, Satoyoshi syndrome, can start in adults and improve with immunosuppressive treatment.

LSD1 and HSP90 help heal skin wounds by changing hair follicle stem cells' metabolism.

Isotretinoin effectively improved severe pityriasis rubra pilaris with complications.

Scalp condition healed with prednisone and tacrolimus.

The specific skin disease variant p.(Arg2000Trp) in plectin can cause a wide range of symptoms, which should be considered when diagnosing patients.

A KRT32 gene variant causes loose anagen hair syndrome.

A specific gene variant (rs4833095) is linked to a higher risk of alopecia areata in Koreans.

Lysophosphatidic acid is important for skin health and disease, and could be a target for new skin disorder treatments.

Gene differences affect finasteride side effects in men with hair loss.

Systemic retinoids may effectively treat erosive pustular dermatosis of the scalp.

Immune cells boost stem cell activity in hairy moles, causing more hair growth.

Poria cocos polysaccharides and finasteride both help treat chronic nonbacterial prostatitis, but Poria cocos polysaccharides also improve gut health.

PCOS is common, affects fertility, and needs early diagnosis and lifestyle changes for management.

EPDS can cause recurring scalp sores and hair loss if not treated.

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

A gene deletion in DSG4 causes sparse hair in some Pakistani families.

A new genetic disorder caused by an ODC1 mutation can be treated with DFMO.

1 alpha,25-dihydroxy-vitamin D3 and calcipotriol speed up cell differentiation in hair follicles.

Certain gene variants can influence acne risk and severity.

Certain genetic changes in the KRT82 gene may cause patchy skin in New Zealand rabbits.

Certain genetic markers linked to reproductive potential were identified by their impact on a protein's ability to bind to genes.

Reducing SFRP1 can promote hair growth and may help treat hair loss.

Smoking and certain health conditions like thyroid disease may make palmoplantar pustulosis harder to treat.

The HSD3B1 variant increases hair loss risk in overweight women with PCOS.

The study found that women with hyperandrogenic PCOS have higher levels of AKT1 and AKT2 proteins in their cells, which may lead to cell dysfunction.

A new genetic mutation in the CAST gene may link PLACK syndrome to alopecia areata.