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Symmetrical Acrokeratoderma (SAK) may be a unique skin condition in China, lacking specific treatment and needing long-term monitoring.

The patient responded well to treatment with no disease progression.

Early diagnosis and aggressive treatment are crucial for managing SLE-related pancreatitis in children.

Some nail changes in chilblains can look like lichen planus and may be severe and long-lasting.

Accurate diagnosis and zinc supplements can improve life quality in acrodermatitis enteropathica, even with normal zinc levels.

Recognizing lupus as a cause of severe gut issues is crucial for effective treatment.

Cronkhite-Canada syndrome is a rare, non-inherited condition causing various symptoms like polyps, hair loss, and weight loss.

Treat limited stage small cell lung cancer with chemotherapy and radiation, and consider preventive brain radiation for better survival chances.

The report described a unique case of Cronkhite-Canada syndrome with unusual polyps and an association with multiple myeloma.

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

Chemotherapy caused nail grooves and separation, but they healed after treatment stopped.

A woman's psoriasis improved after hepatitis C treatment with interferon, despite interferon's risk of worsening skin conditions.

A woman's long-term scalp issues were diagnosed as a rare skin disorder called cutaneous Langerhans cell histiocytosis.

Chemotherapy reduces splenic melanin in mice.

Two patients with Cronkhite-Canada syndrome achieved remission after treatment.

SLE can cause unusual gastrointestinal symptoms, and immunosuppressive therapy can be effective.

Genetic testing confirmed a rare skin disorder in a young girl, which improved with zinc supplementation.

Identical p53 gene mutations in different cancers suggest the need for careful treatment.

Many people with inflammatory bowel disease have a vitamin C deficiency, which can lead to scurvy symptoms.

A rare autoimmune disease caused the woman's scalp blisters and hair loss, successfully treated with medication.

A patient with a PLEC mutation has epidermolysis bullosa, muscular dystrophy, and myasthenia gravis, which improved with steroid treatment.

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.

The cat's skin condition was resistant to treatment and did not improve.

Recurrent pneumothorax can occur in Sjogren's syndrome, even without common markers.

A patient developed a blister at the injection site after hepatitis C treatment.

Relapsing polychondritis might be linked to alopecia areata due to immune system factors.

The research linked PLCD1 gene variants to the development of trichilemmal cysts.

Necrobiosis lipoidica may need new criteria for accurate diagnosis due to similarities with another condition.

New treatments for chronic central serous chorioretinopathy show promise in preventing permanent vision loss.

Active treatment can help prevent scarring hair loss in SLE patients.