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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.

Ashwagandha may improve hormone levels and reduce hair loss in non-classical adrenal hyperplasia.

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

Treating non-classic congenital adrenal hyperplasia is complex because the benefits of hormone treatment must be weighed against potential health risks.

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

Imaging helps detect adrenal gland issues and monitor treatment in congenital adrenal hyperplasia, and can identify tumors affecting fertility.

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.

Natural products may help treat skin inflammation from abnormal adrenal hormones.

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

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

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.

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.

Congenital Adrenal Hyperplasia is a rare inherited disease causing hormone imbalances, affecting growth, fertility, and heart health, diagnosed through blood tests and treated with medication and lifestyle changes.