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Chinese patients with systemic lupus erythematosus commonly experience oral ulcers, arthritis, alopecia, skin rash, and nephritis.

Biotin treatment improves symptoms of biotinidase deficiency, but some neurological damage may be permanent.

Men with systemic lupus erythematosus often have more severe symptoms but can respond well to treatment.

Digital gangrene can be an early sign of late-onset systemic lupus erythematosus.

More skin lesions in lupus patients may indicate higher disease activity.

Leonuri Herba alkaloids may help treat hormone-induced enlarged prostate in rats.

A man had two rare autoimmune diseases that might be connected.

Keratinocytes help manage skin nitrogen metabolism, varying by age and skin area.

Ritlecitinib can reduce inflammation and help hair regrow in Alopecia Areata.

Early immunosuppressive therapy leads to favorable outcomes in Filipino lupus patients with myocarditis.

An 87-year-old man showed unusual signs of Hodgkin lymphoma, primarily high calcium levels, which improved after treatment and revealed the disease.

Timely zinc treatment is crucial for preventing severe complications in Acrodermatitis enteropathica.

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

A man developed temporary hair loss after taking a cancer drug, which might indicate a better treatment response.

Brindled mice show abnormal catecholamine neuron development due to copper deficiency.

Improving cage hygiene and sanitation is crucial to prevent colisepticemia in chickens.

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

Doctors should consider SLE in males even if antinuclear antibody tests are negative.

A specific RNA, circNlgn, contributes to heart damage and scarring caused by the cancer drug doxorubicin.

A 22-year-old with multiple autoimmune diseases needs a multidisciplinary treatment approach.

The A allele of the C2 gene increases the risk of lupus, while the G allele may protect against it.

Two different mutations in the vitamin D receptor gene cause different symptoms and responses to treatment in Lebanese patients with hereditary rickets.

Early diagnosis and individualized treatment improve outcomes for Congenital Adrenal Hyperplasia.

A new genetic mutation was found causing hair and eye issues in a boy.

A genetic mutation caused severe rickets and alopecia in an Indian patient, but high-dose calcium and phosphate treatment improved their condition.

Horses in western Iowa got sick from high selenium in local alfalfa hay.

5-alpha-reductase inhibitors significantly affect the penile tissue of hypertensive rats.

Ritlecitinib is effective and safe for long-term treatment of alopecia areata.

A 13-year-old boy with Cushing syndrome has high cortisol levels from a pituitary gland issue and underdeveloped sexual characteristics.

Chronic autoimmune urticaria can be managed with specific therapies and requires improved diagnosis and treatment methods.