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NISCH syndrome is a rare genetic disorder affecting skin and liver, with variable symptoms and limited treatment options.

Different autoantibody groups in pediatric SLE are linked to specific symptoms and disease outcomes.

A baby boy with 13q deletion syndrome had eye cancer, a woman's vision improved after stopping a breast cancer drug, a man developed cataracts from using Propecia, and a rare skin disorder called Lipoid Proteinosis was discussed. Also, a tool called OCT is useful for diagnosing macular diseases.

Mogamulizumab treatment in Sézary syndrome may cause skin issues and hair loss but can lead to a complete response.

Gender-specific analysis could improve treatment for childhood systemic lupus erythematosus.

A patient with Sézary syndrome showed improvement after treatment and the study suggested follicular mucinosis might indicate future lymphoma risk.

Satoyoshi syndrome can occur without causing premature ovarian failure.

Early detection and multidisciplinary treatment are crucial for managing Papillon-Lefévre syndrome.

SJS/TEN survivors often have severe, overlooked long-term physical problems that are not properly treated after leaving the hospital.

The treatment led to significant hair regrowth in a lupus patient.

Early recognition and aggressive treatment can significantly improve rare ANA-negative lupus with heart and skin issues.

Bardet-Biedl syndrome may include under-recognized skin problems related to its metabolic disturbances.

Clouston Syndrome can be linked to rare sweat gland tumors.

PUVA treatment may have triggered lupus in a woman with psoriasis.

SLE patients in eastern Saudi Arabia have a generally good prognosis despite multi-organ involvement.

A woman with lupus had blood cell destruction, treated successfully with medication.

SLE is rare in Uganda but often has complications and overlaps with rheumatoid arthritis.

A woman had both Graham Little-Piccardi-Lassueur syndrome, causing hair loss, and complete androgen insensitivity syndrome, making her genetically male but physically female. This suggests androgens don't affect the hair loss condition.

A 44-year-old woman with Down's syndrome was diagnosed with both rheumatoid and gouty arthritis and treated with multiple medications.

SH-SY5Y cell lysate is effective for diagnosing Satoyoshi syndrome.

An 80-year-old woman with Cronkhite-Canada syndrome had multiple polyps and symptoms like diarrhea, hair loss, nail issues, and dark skin.

Costovertebral arthritis can cause chronic back pain in SLE patients and needs thorough evaluation.

A patient with Rothmund-Thomson syndrome showed skin changes, hair loss, and dental defects but no cataracts or skeletal issues.

Early diagnosis and treatment of myositis in SLE patients lead to better outcomes.

A 2-year-old boy with a rare brain malformation may have Gomez–López-Hernández syndrome.

Clouston syndrome causes issues with teeth, hair, nails, and skin, and has no cure, but recognition has improved.

Recognizing and treating oral lichen sclerosus is important, but treatment guidelines are lacking.

An 18-year-old girl improved with treatment after being diagnosed with both Systemic Lupus Erythematosus and Celiac Disease.

Infliximab can cause SAPHO syndrome, which may improve with Spesolimab and methotrexate.