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Dermoscopy helped diagnose discoid lupus erythematosus in two patients without needing skin biopsies.

The document reports the first Brazilian case of a girl with Becker nevus syndrome, characterized by skin changes, breast underdevelopment, and scoliosis.

A 36-year-old man had unusual skin lesions on his face without hair loss.

A man developed facial skin lesions after a stem cell transplant, which improved with specific treatments.

A protein called lfTSLP is important in causing allergic and other skin diseases and could be a target for treatment.

A woman with lupus developed a rare skin condition, which improved with increased medication.

KFSD is a rare condition causing scarring hair loss, with no effective treatment known at the time of the report.

Mutations in the DSG4 gene cause specific hair and scalp issues.

Dermoscopy helps diagnose and monitor treatment for hair loss from scarring conditions like discoid lupus and lichen planopilaris.

Certain mouse strains develop a skin condition similar to a human hair loss disease due to genetic defects.

Skin and mucous symptoms are key for diagnosing autoimmune connective tissue diseases.

The document concludes that detailed clinical descriptions of seven family cases help understand dominant dystrophic epidermolysis bullosa's symptoms and inheritance.

Nevoid basal cell carcinomas start in the skin's top layer and hair follicles.

The document concludes that Cutaneous Lupus Erythematosus has different forms, is influenced by genetic and environmental factors, and can be treated with various medications, but more targeted therapies are needed.

A patient with lupus experienced complete hair regrowth after treatment with thalidomide.

Cronkhite-Canada syndrome is a rare condition causing gut polyps, hair loss, skin changes, and nail issues, often with a poor outlook.

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

Cutaneous lupus erythematosus is a common skin condition in lupus, affecting mostly young adult females.

Accurate diagnosis of RDEB-mitis in older adults is crucial for proper management without immunosuppressants.

IVIG therapy significantly improved symptoms in a patient with APS-2 and SPS.

Kindler Syndrome shows diverse symptoms and needs better diagnostic tools and care in resource-limited areas.

The document suggests a rare skin condition might be caused by a genetic phenomenon.

Cronkhite-Canada syndrome is rare, has a poor prognosis, and requires early diagnosis and ongoing treatment.

The document discusses various challenging skin conditions and their treatments.

Lupus affects the body and skin, causing joint pain and skin issues that can be treated with steroids and antimalarial drugs.

The girl's swelling and skin issues improved with fluid restriction and diuretics.

EPDS and MS might share an immune-related cause.

Scalp sarcoidosis can cause hair loss and needs accurate diagnosis and treatment with specific medications.

A rare form of lupus caused hair loss and skin bumps, diagnosed through biopsy, improved partially with treatment.

Older men's scalp damage increases with age and sun exposure, a baby girl in the Philippines has Schimmelpenning syndrome, and thyroid screening is advised for children with hair loss and certain risk factors.