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Small bowel lesions in Cronkhite-Canada syndrome persist despite steroid treatment.

The document concludes that HAIR-AN syndrome should be considered when a patient shows severe hyperandrogenism and insulin resistance after excluding tumors.

Benign ovarian tumors can cause excess male hormones and related conditions in postmenopausal women.

The document concludes that diagnosing and treating Congenital Adrenal Hyperplasia is complex and requires a team approach due to its effects on the skin and other symptoms.

Pimozide treatment resolved cysts and partially restored cheek fat in a man with Barraquer–Simons 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.

The patient had complex urinary tract issues and ambiguous genitalia, with physical features suggesting a hormonal imbalance.

Congenital Adrenal Hyperplasia is mainly caused by enzyme deficiencies, leading to varying symptoms like hormone imbalances and physical changes.

An elderly man had a rare, large skin cyst on his lower back, which was removed by surgery.

Some women with excess hair growth have a hormone condition that can't be diagnosed by blood or urine tests alone.

Ulcerative sarcoidosis in body folds is rare and improved with prednisone and hydroxychloroquine.

Cortisol increases a specific protein in bone cells, which may help explain its negative effects on bone.

Trilostane effectively and safely treats dogs with pituitary-dependent hyperadrenocorticism, improving symptoms and adrenal gland size.

Bilateral ovarian hyperthecosis is a rare but treatable cause of increased facial hair in postmenopausal women.

Surgery removed ovarian tumors, normalizing testosterone and improving symptoms.

Surgical removal of a rare ovarian tumor improved symptoms and hormone levels in a postmenopausal woman.

Trilostane generally improved symptoms in dogs with Cushing's syndrome, but dosage adjustments were needed over time.

Surgery removed an ovarian tumor, improving her symptoms and normalizing testosterone levels.

Untreated congenital adrenal hyperplasia can lead to complications like stroke and needs glucocorticoid treatment.

Cronkhite-Canada syndrome is rare, has a poor prognosis, and requires early diagnosis and ongoing treatment.

Taking thyroid medication reduced the patient's pituitary gland swelling and improved her symptoms.

A patient with HAIR-AN syndrome, PCOS, and Hashimoto's thyroiditis improved with early diagnosis and treatment to prevent serious health problems.

The modified Crawford technique resulted in less lagophthalmos and better cosmetic outcomes for patients with lateral droop.

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

Non-classic congenital adrenal hyperplasia (NCCAH) can mimic PCOS and requires genetic testing for proper diagnosis and treatment.

Hair hormone levels can indicate obesity-related changes and are useful for research and clinical practice.

A rare ovarian tumor caused high male hormone levels, but surgery fixed it.

Confinement in farrowing crates doesn't increase chronic stress in sows, but hair cortisol measurements may not reliably indicate stress due to hair growth variations.

A person with thyroid problems had rare, swollen, bald spots on their scalp caused by a condition usually found on the shins.

A rare ovarian tumor caused a postmenopausal woman to develop male-like features, which improved after surgery.