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Non-classic congenital adrenal hyperplasia is a common disorder causing symptoms like acne and infertility, and it's managed based on symptoms, not just test results. Treatment can improve fertility and reduce miscarriage risk.

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.

Testing basal 17-HP levels is a good way to screen for nonclassic adrenal hyperplasia in women with high androgen levels.

Women with nonclassic 21-hydroxylase deficiency can have successful pregnancies through IVF, with certain factors affecting their chances.

A postmenopausal woman's masculine symptoms improved after surgery for a hormone-producing ovarian tumor.

Minoxidil affects collagen-related genes, potentially helping treat fibrosis.

Scientists found a new gene in a bacterium that can modify an immunosuppressant drug, potentially helping to treat hair loss.

LC-MS/MS is more reliable than immunoassays for diagnosing 21-hydroxylase deficiency.

11α-Hydroxyprogesterone is changed into different substances by certain enzymes and may play a role in prostate cancer.

Late diagnosis of congenital adrenal hyperplasia can greatly affect physical development, gender identity, and sexual health.

Certain drugs that block specific enzymes can help treat prostate diseases.

Shorter CAG repeats in a specific gene may increase male hormone activity and symptoms like acne and excess hair in women with PCOS.

Two rare genetic diseases cause severe rickets in children due to defects in vitamin D metabolism.

Vitamin D receptor is crucial for bone health and mineral metabolism.

Acne significantly affects mental health and quality of life, with research suggesting hormonal and genetic factors in its development and emphasizing early treatment to prevent scarring.

Hormone imbalances can cause specific skin changes, which may help in early detection of endocrine disorders.

A woman's mature cystic teratoma caused her virilization by producing testosterone.

Adding soybean oil to Nonomuraea dietziae increases production of a beneficial compound by improving metabolism and enzyme systems.

Brothers of women with PCOS tend to have higher levels of a hormone called DHEAS, indicating a possible genetic link.

APS-1 in Italy shows diverse AIRE mutations and various autoimmune issues.

Mice without the vitamin D receptor have bone issues and other health problems, suggesting vitamin D is important for preventing various diseases in humans.

Obese Hispanic women with PCOS are at higher risk for metabolic problems than non-Hispanic white women.

The document concludes that treatment for excessive hair growth depends on the cause, with options including hair removal methods and medications like anti-androgens or insulin-sensitizing drugs.

New treatments are needed for PCOS that target its genetic, hormonal, and metabolic causes.

The document concludes that more research is needed to understand excessive hair growth in women with normal hormone levels and regular ovulation.

A new gene mutation causes female pseudohermaphroditism due to glucocorticoid resistance.

Minoxidil reduces lysine hydroxylase in skin cells.

Gene mutations can cause problems in male genital development.

Exposure to too much androgen before birth might cause polycystic ovary syndrome later in life.

Male pattern baldness is mostly inherited, involves many genes, and is linked to other traits like early puberty and strong bones.