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Gene mutations can cause problems in male genital development.

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.

Treating non-classic congenital adrenal hyperplasia is complex because the benefits of hormone treatment must be weighed against potential health risks.

Mutations in the vitamin D receptor cause hereditary vitamin D-resistant rickets, leading to poor bone health and requiring high calcium doses for treatment.

Cirrhosis affects quality of life with various symptoms, requiring a holistic, multidisciplinary approach for management.

Most dogs with adrenal-dependent hypercortisolism had normal blood pressure after one year of treatment or surgery.

Finasteride worsens heart damage from nandrolone decanoate but protects against cell damage.

Follicle Stimulating Hormone is important for fertility.

Minoxidil controls blood pressure effectively, but may cause side effects like hypertrichosis.

The document concludes that treating androgen excess needs patience, managing expectations is important, and many drugs used are not officially approved, suggesting cosmetic options for mild cases.

The conclusion is that endocrinology significantly impacts medicine with various common medications used for treatment.

Minoxidil affects rat fluid dynamics, altering pressure and circulation, improving blood flow and hair growth.

Children with classic congenital adrenal hyperplasia have thicker heart fat and are at higher risk for heart problems and early atherosclerosis.

A woman's small, unnoticed adrenal mass turned out to be a rare non-Hodgkin's lymphoma, treated successfully with surgery and therapy.

Children with classic congenital adrenal hyperplasia have thicker heart fat and more heart and blood vessel risk factors, especially if their condition is not well-controlled.

Itraconazole is potentially effective for treating invasive aspergillosis, but more research is needed.

Lower SHBG levels may increase the risk of PCOS.

Treatment can improve survival and symptoms in dogs with Cushing's disease, but outcomes are unpredictable.

Stopping minoxidil and draining fluid around the heart can save lives in rare cases.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

Poor maternal nutrition can lead to fewer wool follicles in Chinese Merino sheep.

The conclusion is that more research is needed to better understand and treat adult acne, and that patient education and simple treatment plans are important for better results.

A woman's rare benign tumor that released both cortisol and testosterone was successfully removed, improving her health.

A woman with anorexia developed gout from self-induced vomiting.

Overexpressing the mineralocorticoid receptor in mouse skin causes skin thinning, early skin barrier development, eye issues, and hair loss.

A woman was diagnosed with a rare adrenal gland cancer that did not show usual hormone-related symptoms.

New methods to make oxasteroids show promise for medical treatments like osteoporosis and breast cancer.

Researchers created a mouse model for Cushing's syndrome to study glucocorticoid excess and potential treatments.

Some oral medications may help treat central serous chorioretinopathy, especially eplerenone, but more research is needed.

A man with hypoparathyroidism had other health issues that led to a diagnosis of a rare autoimmune disorder, APS-1.