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A teenage girl had both a rare ovarian tumor and a severe form of polycystic ovarian syndrome.

Long-term data and a team approach are needed to manage chronic side effects from cancer treatments.

NonClassic Congenital Adrenal Hyperplasia is a less severe form of a genetic disorder affecting adrenal gland function.

Corticosteroids are the most effective treatment for Satoyoshi syndrome.

Identifying nonclassic congenital adrenal hyperplasia and carriers of CYP21 mutations is challenging, and genetic counseling is recommended due to their prevalence.

A misdiagnosed case of HAIR-AN syndrome led to unnecessary surgeries and highlighted the importance of correct diagnosis and treatment.

Patients with central centrifugal cicatricial alopecia often have higher rates of metabolic, autoimmune, and atopic conditions, as well as anxiety and depression.

An 80-year-old man with COVID-19 also had constrictive pericarditis, possibly due to an autoimmune or immunoglobulin related disease, and improved after surgery.

A 56-year-old man was diagnosed with Cronkhite-Canada Syndrome after showing symptoms like diarrhea, weight loss, and skin changes.

A Laotian man with unusual skin changes and multiple growths in his gut was diagnosed with Cronkhite-Canada Syndrome and improved with nutritional and immune-based treatments.

Non-classic congenital adrenal hyperplasia is a common disorder causing symptoms like acne and infertility, and it's managed based on symptoms, not just test results. Treatment can improve fertility and reduce miscarriage risk.

Cardiovascular drugs can cause various skin problems, so recognizing these reactions is important.

A rare autoimmune condition, Satoyoshi syndrome, can start in adults and improve with immunosuppressive treatment.

CRPS type I is a complex pain condition with no proven cure, requiring personalized treatment.

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

First Korean case of Cronkhite-Canada syndrome with colon cancer and serrated adenoma.

Hirsutism and androgenetic alopecia in women are often due to increased androgen effects, and antiandrogen treatment is recommended to prevent further issues.

A woman was the first known case to have both polycystic ovary syndrome and autoimmune polyglandular syndrome type 2, suggesting a need to check for both conditions in similar patients.

Cronkhite-Canada syndrome is rare, with high mortality and cancer risk, needing more research for treatment guidelines.

Using anabolic steroids 'Sus' and 'Deca' for bodybuilding caused severe acne in a man.

DCP therapy causes side effects like weakness, flushing, headaches, and taste changes, but less frequently causes hypertension and diabetes.

Certain liver diseases respond well to specific treatments and have varying risks for liver cancer.

Postmenopausal women with excess male hormones may have ovarian tumors, and surgery usually cures them.

Mixed Connective Tissue Disease can develop from overlapping symptoms of several autoimmune diseases, making diagnosis complex.

Sulfasalazine can cause severe allergic reactions leading to long-term autoimmune issues like hair loss and skin discoloration.

Satoyoshi syndrome is likely an autoimmune disease.

Type B Insulin Resistance Syndrome is rare, linked to lupus, and hard to treat due to severe insulin resistance.

A man's rare adrenal tumor caused feminization and white hair, was removed surgically, and improved after treatment.

Two transplant patients on cyclosporine unexpectedly developed hair loss.

A man developed skin lesions as a side effect of a gamma secretase inhibitor used for treating a tumor.