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

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

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

A woman's severe hormone imbalance after menopause led to finding a rare ovarian tumor, treated by surgery.

Diagnosing sex development disorders requires combining medical history, physical exams, imaging, lab tests, and genetic data.

Understanding how DHT works is important for diagnosing and treating hormone-related disorders.

A woman with a specific mutation causing adrenal gland issues faced fertility problems, but careful hormone therapy helped her manage it successfully.

Siblings with signs of virilization should be tested for non-classical congenital adrenal hyperplasia, which does not affect adult height but may impact fertility and well-being if untreated.

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.

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

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

Two women with very high androgen levels had only slight skin issues, one due to a non-classical adrenal disorder and the other due to an adrenal tumor.

Most women referred for excess male hormone symptoms had polycystic ovary syndrome (PCOS), with other conditions being less common.

People with reproductive, thyroid disorders, and type 2 diabetes can experience voice changes, but more research is needed to understand this better.

Some parents have a mild form of congenital adrenal hyperplasia without symptoms, and they usually don't need treatment.

Hair steroid measurement is an effective method to diagnose and monitor CAH in developing countries.

A woman's hyperandrogenism was caused by a genetic mutation leading to non-classic adrenogenital syndrome.

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.

Early adrenal gland maturation in young children can be normal, but other serious conditions should be ruled out first.

The study concluded that androstendione and DHEA are important for diagnosing high male hormone levels in women with excessive hair growth.

To diagnose Polycystic Ovarian Syndrome, two out of three signs—irregular periods, high male hormone levels, or cysts on the ovaries—are needed.

The document concludes that careful evaluation is needed to diagnose PCOS correctly due to similar symptoms in other conditions, and accurate testosterone level measurement is crucial.

Androgens like testosterone are important hormones for both men and women, made differently in each sex and affecting the body by regulating genes and quick interactions with cell components.

Hormonal treatment is effective for women with acne not helped by usual treatments, especially if they have hormonal imbalances.

Greek women with classic PCOS are more likely to have metabolic syndrome and insulin resistance than those with newer PCOS types.

Adrenal disorders can cause lasting brain and behavior issues in children.

The document concludes that identifying the cause of amenorrhea is crucial for proper treatment.

Genes and epigenetic changes are important in the development of Polycystic Ovary Syndrome.

The document concludes that early recognition and treatment of PCOS in adolescents is crucial for managing symptoms and long-term health risks.

People who carry the 21-Hydroxylase Deficiency gene are not more likely to have excessive male hormone levels.