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Measuring 17-hydroxyprogesterone in hair can help monitor androgen levels in people with congenital adrenal hyperplasia.

Certain adrenal hormones can strongly stimulate oil gland growth in hamster skin, similar to male hormones.

Glucocorticoid and mineralocorticoid therapy effectively manage Congenital Adrenal Hyperplasia symptoms but have limitations.

Women with non-classical congenital adrenal hyperplasia have higher levels of certain steroids, which can be reduced by treatment.

A woman's symptoms of increased body hair and testosterone were caused by a rare adrenal tumor, which was removed successfully.

Women with congenital adrenal hyperplasia (CAH) have more sexual function issues than those with polycystic ovary syndrome (PCOS), but physical activity can improve sexual functioning in all women.

GnRH analogue can help diagnose ovarian causes of high testosterone in postmenopausal women when scans don't show the cause.

Low DHEA-S levels might be linked to alopecia areata and could be a potential treatment target.

Some women with excess hair growth have a hormone condition that can't be diagnosed by blood or urine tests alone.

Women with a certain type of tumor had higher levels of pregnancy hormone and male hormones, which decreased after treatment.

Diagnosing simple-virilizing congenital adrenal hyperplasia can be difficult and requires thorough testing and expert advice.

A 70-year-old woman with a malignant adrenal tumor improved after surgery and radiotherapy.

Early hormones shape sex-specific differences in rat glands.

Higher androgen levels during puberty are linked to shorter adult height in boys with Silver-Russell syndrome.

Venous catheterization may help diagnose the cause of female hyperandrogenism when imaging is unclear.

Removing both ovaries treated the woman's excess male hormone symptoms.

21-hydroxylase deficiency causes hormone imbalances leading to various symptoms, and diagnosis involves clinical and genetic tests.

A thorough diagnostic process and teamwork are crucial for managing complex hyperandrogenism in postmenopausal women.

Most dogs with adrenal-dependent hypercortisolism had normal blood pressure after one year of treatment or surgery.

Removing an adrenal tumor can significantly reduce high androgen levels in postmenopausal women.

A 13-year-old girl's masculine symptoms improved after surgery for a rare adrenal tumor that produced male hormones.

A rare adrenal tumor in a woman only made DHEA-S, causing hair thinning, and was removed, fixing the hormone level.

Using GnRHa agonists helps diagnose and treat ovarian hyperthecosis when surgery isn't possible.

A woman's adrenal tumor disappeared after treatment with cyproterone acetate.

A woman's Cushing's syndrome caused by adrenal cancer improved after surgery.

Intralesional steroid injections can effectively treat calcinosis and ulcers in scleroderma.

High androgen levels and genetic factors likely cause Becker's nevus and related symptoms.

Nonclassic congenital adrenal hyperplasia is a genetic disorder causing hormone imbalances, affecting fertility and requiring personalized treatment.

Rare adrenal cancers that secrete androgens or estrogens have a poor prognosis and are treated primarily with surgery.

Children with classic congenital adrenal hyperplasia have thicker heart fat and are at higher risk for heart problems and early atherosclerosis.