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

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

Nonclassic congenital adrenal hyperplasia is a genetic disorder causing hormone imbalances, affecting fertility and requiring personalized treatment.

Early diagnosis and individualized treatment improve outcomes for Congenital Adrenal Hyperplasia.

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.

Enzymes are classified into six types and are essential for many biological processes, with only a few targeted by drugs.

The skin's ability to produce hormones is linked to various skin conditions, and better understanding this process could lead to new treatments.

Genetic mutations can affect female sexual development, requiring personalized medical care.

Women with androgen excess, especially those with PCOS, have a much higher risk of heart disease and stroke.

A genetic marker linked to a type of hair loss was found in most patients studied.

Hyperadrenocorticism in ferrets is linked to neutering and indoor housing, and is best treated with surgery and a deslorelin implant.

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

Using 17-hydroxyprogesterone levels to diagnose nonclassic congenital adrenal hyperplasia can result in many incorrect diagnoses.

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

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

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

The document concludes that Nonclassic Congenital Adrenal Hyperplasia requires personalized treatment plans to manage symptoms and fertility, with glucocorticoids being a common therapy.

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

About 2.2% of women with symptoms of high male hormones have a mild form of congenital adrenal hyperplasia, and measuring a specific hormone level can accurately diagnose it.

Molecular diagnostics help identify genetic defects causing endocrine diseases, improving diagnosis and treatment options.

Women with hyperandrogenism have higher androgen levels and lower SHBG, which may contribute to conditions like excessive hair growth and early puberty.

Gastric bypass surgery improved a woman's hormonal disorder without the need for medication.

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

The report concludes that PCOS is mainly a condition of excess male hormones and its definition may change as new information is discovered.

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.

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

Minoxidil slows fibroblast growth and collagen production, potentially treating keloids, hypertrophic scars, and connective tissue disorders.

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

FA2H is essential for normal fur and sebum production in mice.

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