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The S250C variant in a gene may cause autoimmunity and immunodeficiency by impairing protein function.

The medication cyproterone acetate/ethinylestradiol is usually prescribed correctly for acne after other treatments don't work.

Cyproterone acetate is used to treat conditions like prostate cancer, early puberty, excessive sexual drive, and female androgenization by blocking male sex hormones.

Arab APS1 patients have unique and recurrent AIRE gene mutations.

Compounds 15, 20, and 25 are strong inhibitors of human steroid 5α-reductase type 2.

Genetic factors play a major role in acne.

A KRT32 gene variant causes loose anagen hair syndrome.

A compound from brown algae boosts the production of a certain inflammatory substance in skin cells.

Albumin and prednisone improved symptoms in a woman with Cronkhite-Canada syndrome, revealing potential genetic causes.

A male with aromatase deficiency improved bone health with estradiol treatment.

Women with excessive hair growth or polycystic ovary disease may more often carry a gene variant for 21 hydroxylase deficiency.

TMPRSS2 is crucial for COVID-19 infection and is a potential target for treatment.

ETC-159 was safe up to 30 mg, but no tumor shrinkage was seen.

Cyproterone acetate is used for topical treatment of diseases dependent on male hormones.

A new goat gene affects cashmere fiber thickness; certain variations can make the fibers coarser.

Lowering homocyst(e)ine levels can reverse skin and hair lightening by restoring enzyme activity needed for pigmentation.

A new gene mutation caused a man's rare skin condition, Schöpf-Schulz-Passarge syndrome.

An 11-year-old Greek girl was diagnosed with a rare genetic disorder, highlighting the importance of genetic testing and family history.

Overexpression of hurpin in mice leads to abnormal skin and higher skin cancer risk.

Researchers found two enzymes in Avicennia marina that help produce maslinic acid and corosolic acid, which have medicinal benefits.

Researchers developed a method to identify and analyze cyclosporin compounds and their structures effectively.

Changing the C-ring structure in certain compounds can make them better at blocking a specific human enzyme.

CT60 polymorphism might increase the risk of Alopecia Areata.

Longer CAG and GGN repeats increase alopecia risk, but no significant link to post-finasteride syndrome found.

Hirsute women have lower type 2 17β-HSD enzyme levels, which improve with treatment.

Two different mutations in the vitamin D receptor gene cause different symptoms and responses to treatment in Lebanese patients with hereditary rickets.

Three genes linked to the development of trichilemmal cysts were found.

Certain gene variants are linked to a higher risk of polycystic ovary syndrome, hair loss, and obesity in women from western Saudi Arabia.