Search

everythinglearnresearchcommunity

for

Search:↓

A new gene variant causes glucocorticoid resistance in a mother and son.

Topical corticosteroids may be a safe and effective treatment for severe alopecia areata in children.

A Cavalier King Charles Spaniel had both uveodermatological syndrome and alopecia areata, and treatment with ciclosporin helped regrow hair.

A woman with Sheehan syndrome improved with hormone treatment.

Cronkhite-Canada syndrome can sometimes show unusual colonic adenomatous polyps.

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

Early diagnosis and treatment of NCCAH can improve symptoms and fertility.

Imaging helps detect adrenal gland issues and monitor treatment in congenital adrenal hyperplasia, and can identify tumors affecting fertility.

The patient with a misplaced pituitary gland and interrupted pituitary stalk is being treated with hormone replacement.

Clouston syndrome can lead to skin cancer, so monitoring is crucial.

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

A rare scalp condition causing hair loss improved with a specific cream.

A toddler with a rare adrenal gland tumor causing male-like physical changes was successfully treated with surgery.

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

Immunotherapy for cancer caused a patient to develop a condition affecting hormone production, requiring ongoing hormone replacement therapy.

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

Clouston Syndrome can be linked to rare sweat gland tumors.

Intralesional steroid injections can effectively treat calcinosis and ulcers in scleroderma.

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.

Trilostane helped a cat with a hormone issue but the cat later died from a kidney infection.

The conclusion is that thorough investigation of hypertension and hormonal dysfunctions is important, and there may be a link between these conditions and cancer.

Early intervention is important for limited systemic sclerosis patients due to higher pain and ulceration risks.

A woman had a rare liver tumor causing male-like physical changes, highlighting the need for thorough checks when such symptoms appear.

Hair samples can't reliably detect hypercortisolism in anorexia nervosa patients.

A new medical syndrome may include skin changes, hair loss, sweating issues, bone malformations, leg swelling, and low cortisol.

Men with Addison disease should be screened for X-linked adrenoleukodystrophy if they have hair loss.

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

A 21-year-old male with a rare genetic disorder experienced sudden hair loss and high DHEAS levels, likely due to a condition similar to PCOS, usually seen in women.

Inflammation may cause nail issues in Cronkhite–Canada Syndrome.

The patient with both scarring and non-scarring hair loss showed complex immune reactions and improved with steroid treatment.