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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.

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.

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.

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.

Early hormones shape sex-specific differences in rat glands.

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

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

A man's health improved after treating his undiagnosed adrenal insufficiency, which caused fatigue and weight loss.

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.

A patient produced cortisol after adrenalectomy, possibly due to residual tissue or other body parts making steroids.

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.

The document concludes that patient outcomes for Congenital Adrenal Hyperplasia are often not ideal because of poor management and a need for better diagnosis and treatment methods.

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