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Glioblastoma cells can make androgens, which might help the tumor grow.

The girl's unexpected pubic hair growth led to a diagnosis different from complete androgen insensitivity syndrome.

Genetic factors, skin barrier, immune function, and obesity influence risk of fungal skin infections.

Lack of certain cells causes abnormal nipple development and nursing failure.

DHT in the human prostate is produced through multiple pathways, not just from testosterone.

Evaluate and manage androgen excess in women with a systematic approach, considering both physical and psychological impacts.

Two enzymes regulate androgen receptor activity, affecting treatments for androgen insufficiency and benign prostatic hyperplasia.

Oxidative stress worsens PCOS by damaging cells and disrupting metabolism, suggesting antioxidant treatments might help.

Prostate cancer can progress even with low testosterone due to internal hormone production in the tumor.

Fetal ovaries produce different hormones than adult ovaries, and endocrine-disrupting chemicals may affect this process.

Diet changes hormone levels in pregnant ewes by affecting metabolism, not placental synthesis.

Mice without the enzyme HSD17B3 still produce normal testosterone, suggesting they have different ways to make it compared to humans.

Hirsutism in GCC countries is influenced by genetics, obesity, and lifestyle, with cultural stigma delaying treatment, highlighting the need for tailored health strategies.

Androgens are important for female fertility and could help in IVF treatment, but also play a role in causing PCOS.

High androgen levels cause skin issues in PCOS, affecting quality of life.

Gut bacteria affect steroid levels, influencing health conditions and potential treatments.

An ovarian tumor can cause high male hormones in postmenopausal women.

Different types of PCOS need specific diagnosis methods and treatments.

A patch with curcumin-zinc can improve hair growth and health by delivering beneficial particles to the skin, increasing hair follicles, and reversing effects of a hair loss hormone.

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

Certain variations of the HDAC9 gene can increase or decrease stroke risk in the Chinese population.

A genetic mutation in a specific gene causes a salt-wasting condition in a Pakistani girl and her family.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

A rare gene variant causes sexual development issues in siblings, needing personalized treatment.

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

The PER3 rs772027021 SNP may cause mild skin pigmentation changes in a new subtype of dyschromatosis universalis hereditaria.

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

A genetic defect causes males in some Mediterranean populations to be born with ambiguous genitalia and develop male traits at puberty.

A specific gene variation increases the risk of high uric acid and cholesterol in young Mexican males.

Researchers found genetic mutations causing hypohidrotic ectodermal dysplasia in 88% of studied patients and identified new mutations and genetic variations affecting the disease.