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A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

A 4-year-old girl with a rare lupus condition was successfully treated with oral corticosteroids, leading to full recovery and hair regrowth.

A 60-year-old man with Cronkhite-Canada syndrome improved with treatment, but the condition has a high mortality rate and a risk of colorectal cancer.

Silicon may affect calcium metabolism in dialysis patients, causing symptoms like skin eruptions and abnormal hair growth.

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

A man with a weakened immune system was diagnosed with a rare skin condition called trichodysplasia spinulosa using skin examination techniques.

Accurate diagnosis of SLE requires extensive testing due to its complex symptoms.

Catalytic antibodies are early indicators and active participants in the development of systemic lupus erythematosus.

Prednisolone improved symptoms in a woman with Cronkhite-Canada syndrome, but regular screenings are needed due to cancer risk.

A man with Cronkhite-Canada syndrome had all 20 nails detach but improved with treatment.

An 11-year-old girl with a rare skin disorder also had cornea issues and dry eye, needing careful management.

A family was found with both Trichorhinophalangeal syndrome and Loose Anagen Syndrome, suggesting a genetic connection.

Traditional Chinese medicine may help relieve symptoms of Cronkhite-Canada syndrome.

Nilotinib can cause generalized keratosis pilaris.

Cyclosporine-A can cause excessive hair growth, which usually stops after discontinuing the drug.

Two patients treated with TAC for mouth fibrosis improved but developed Cushing's Syndrome symptoms.

Skin issues are common in lupus patients, highlighting the need for thorough skin checks.

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

A woman with dermatomyositis showed rare skin symptoms, was treated successfully, and her case suggests checking for cancer in similar patients.

The condition might be caused by genetic changes after birth.

A 16-year-old girl with autoimmune hemolytic anemia and deep vein thrombosis improved with treatment, possibly indicating systemic lupus erythematosus.

Long COVID in Japan involves persistent symptoms like fatigue and may be caused by lasting organ damage and prolonged inflammation, with vaccination as a potential treatment.

Carriers of a specific gene mutation have subtle skin changes without visible symptoms.

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.

The boy's symptoms suggest a possible new medical condition.

Non-itchy rashes can indicate serious diseases like lupus.

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

Systemic lupus erythematosus is managed with lifestyle changes, symptomatic treatments, and careful use of medications to control symptoms and flares.

Ruxolitinib treatment may cause eyelash growth.