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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.

Finasteride, when taken daily, lowers dihydrotestosterone levels but doesn't noticeably affect adrenal steroid production, except by blocking the 5 alpha-reductase enzyme.

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.

Goat hair shows changes in metal levels and stress when goats move from indoors to mountain pastures.

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

A woman developed Cushing syndrome and adrenal insufficiency from using fluticasone and ritonavir together.

The conclusion is that thorough investigation of hypertension and hormonal dysfunctions is important, and there may be a link between these conditions and cancer.

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.

A boy's hair loss improved after tumor removal and vitamin D treatment, but hair loss returned despite normal vitamin D and no tumor regrowth.

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

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

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

A rare case of Cushing syndrome was successfully treated with one-sided adrenal gland removal, suggesting personalized treatment is important.

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

A boy with a new NR5A1 gene mutation has a sex development disorder without affecting his adrenal glands.

Long-term treatment with buprenorphine/naloxone for opioid addiction may lead to secondary adrenal insufficiency.

The case shows the importance of quick and thorough evaluation of adrenal tumors to prevent rapid disease progression and poor outcomes.

Long-term opioid use can cause a serious condition where the adrenal glands don't work properly, which doctors should watch out for.

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 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.

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

A genetic marker linked to a type of hair loss was found in most patients studied.

Ectopic adrenal rests can cause androgen excess after adrenalectomy and may need targeted surgery.