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A woman with lupus improved significantly from scalp hair loss after treatment, highlighting the need to identify psoriatic alopecia in lupus patients to avoid permanent hair loss.

JSLE patients often have more hormone and metabolism issues, so regular check-ups and preventing obesity can help.

COVID-19 may trigger systemic lupus erythematosus, requiring careful diagnosis and treatment.

Gender affects the symptoms and severity of systemic lupus erythematosus.

Minimally invasive glaucoma surgery can effectively manage glaucoma in GAPO syndrome when other treatments fail.

A woman with severe hair loss due to systemic sclerosis regrew her hair in 4 months using a combination of treatments.

A rare case links early-onset alopecia universalis and nephrotic syndrome, suggesting genetic immune issues.

EGFR and mTOR inhibitors may help manage Olmsted syndrome symptoms.

Genetic testing is crucial for diagnosing and treating acrodermatitis enteropathica effectively.

The case shows how hard it is to tell apart Multiple Autoimmune Syndrome from other similar autoimmune conditions, but correct diagnosis is key for treatment to work.

An 87-year-old woman was diagnosed with type 3 autoimmune polyendocrine syndrome and had multiple autoimmune issues.

COVID-19 may trigger severe skin flare-ups in people with autoimmune conditions like lupus.

SJS and TEN can cause long-term organ damage and psychological issues beyond skin and eye problems.

Tjalma Syndrome is a rare condition in people with lupus, causing fluid buildup and high CA-125 levels, but not due to tumors.

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

Genetic screening is crucial for accurately diagnosing APS-1 due to its varied symptoms.

Skin symptoms in lupus help diagnose and manage the disease early.

Rituximab may be an effective treatment for Cronkhite-Canada syndrome with kidney disease.

Early treatment of pediatric lupus-related eye issues is crucial to prevent vision loss.

Rash in SLE patients indicates more severe disease.

Blocking the NOTCH pathway can prevent fibrosis in systemic sclerosis.

The patient was diagnosed with oral lichen sclerosus and needs long-term monitoring.

Clouston syndrome is inherited in an autosomal dominant pattern and caused by a specific gene mutation, with no current treatment available.

Erosive lichen sclerosus is a distinct subtype with specific skin features, and treatment led to complete resolution in half of the cases.

CSC is linked to mineralocorticoid receptor damage, stress, and steroid use, with treatments including drugs and laser therapies to prevent eye damage.

Dystonia may be part of PAS-4 and linked to immune issues.

No single biomarker is reliable enough for diagnosing and assessing SLE.

Anti-SRP myopathy can be linked to systemic lupus erythematosus and may improve with specific treatment.

Intralesional cidofovir may be a viable alternative treatment for SCC.

Pincer nails are rare in lupus patients and may be managed conservatively.