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

Women with non-classic congenital adrenal hyperplasia have higher risk for heart and metabolic problems.

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

Early detection of ovarian steroid cell tumors is crucial to prevent lasting symptoms.

Ovarian steroid cell tumors can mimic adrenal hyperplasia, and surgery can normalize hormone levels.

Certain genetic variants reduce enzyme activity, contributing to non-classic congenital adrenal hyperplasia.

Certain genetic variants impair enzyme activity, contributing to non-classic congenital adrenal hyperplasia.

The patient with severe hirsutism improved after being diagnosed with non-classic congenital adrenal hyperplasia and treated with corticosteroids.

A new mutation in the CYP11B1 gene was found in a woman with mild hyperandrogenemia, a rare cause of non-classic congenital adrenal hyperplasia.

Ashwagandha may improve hormone levels and reduce hair loss in non-classical adrenal hyperplasia.

New genotype linked to non-classical congenital adrenal hyperplasia found in Italian siblings.

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.

The article concludes that hormonal therapy is an effective long-term acne treatment, even for those without hormonal imbalances.

Almost half of the dermatology patients in Eastern Turkey use alternative medicine, which can be risky and delay proper treatment.

Most women with excess male hormones have Polycystic Ovary Syndrome, and hormonal therapy can improve symptoms but may cause side effects.

The definition of Polycystic Ovary Syndrome may change with new research, and careful screening is key for managing the condition.

The document concludes that hirsutism is the main sign for diagnosing hyperandrogenism, which requires a detailed patient history and physical exam.

Some alternative treatments for hair loss might work, but more research is needed.

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

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

With careful management, people with congenital adrenal hyperplasia can have successful pregnancies and become parents.

Hirsute women have lower type 2 17β-HSD enzyme levels, which improve with treatment.

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

Flutamide works better than finasteride for hirsutism, and combining both is slightly better but not much.

Blood tests are needed to confirm high male hormone levels in women with PCOS, as physical signs alone are not reliable.

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

Low-dose anti-androgen drugs and certain drug combinations are effective for hirsutism, and insulin sensitizers show promise, especially for those with polycystic ovarian syndrome.

Mutations in the CYP21A2 gene are not a major factor in causing PCOS.

Antiandrogens are the main treatment for hirsutism, with individualized care and safe, affordable options needed.

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.