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The study concluded that testing hormone levels after stimulation is not reliable for identifying carriers of 21-hydroxylase deficiency; genetic testing is necessary.

CAH is a genetic disorder affecting cortisol production and causing hormonal imbalances, with treatment and diagnosis varying by form and symptoms.

Adrenal glands delay the start of winter fur growth in mink.

Women with congenital adrenal hyperplasia have lower fertility, but with proper treatment, they can conceive successfully.

Women with nonclassic congenital adrenal hyperplasia experience more sexual dysfunction and distress.

A woman with a rare adrenal tumor and hormonal disorder had improved testosterone levels after surgery, but her menstrual irregularities continued.

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.

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.

Most adrenal cortex tumors are benign and non-secreting, but proper diagnosis and treatment are important due to the rare possibility of cancer.

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.