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Educating primary care doctors and improving referrals to rheumatologists can reduce delays in treating lupus patients.

Alopecia can be caused by multicentric reticulohistiocytosis.

People with lupus in Mauritius face many challenges and need more support and understanding.

A genetic mutation in the CDH3 gene causes hair loss and vision problems in a young Saudi girl.

DCPA is a chronic leg infection often related to Staphylococcus aureus, affecting mostly young men in India.

The document concludes that anticonvulsants like phenytoin may cause skin reactions by affecting tryptophan metabolism and suggests researching vitamin levels in patients with drug reactions.

The document concludes that syphilis has varied symptoms that are often missed, making clinical awareness crucial for diagnosis.

Salmon patches on the neck may relate to the severity and recurrence of alopecia areata.

Inflammation may cause nail issues in Cronkhite–Canada Syndrome.

Netherton Syndrome is a non-treatable genetic disorder in children causing skin, hair, and allergy issues.

Chronic scarring alopecia is common in SLE patients and needs early detection and management.

Genetic variants in PDE6H and LPAR6 cause vision impairment and hair loss in two Pakistani brothers.

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

CRPS I is complex, linked to immune and nerve issues, and needs comprehensive treatment.

A woman's hair loss and skin discoloration were found to be caused by a rare case of leprosy on the scalp, not alopecia-vitiligo overlap.

Skin problems can indicate different diseases inside the body.

COVID-19 vaccination may be linked to MIS-C in children, highlighting the need for quick diagnosis and treatment.

Changes in the SREBF1 gene cause a rare genetic skin and hair disorder.

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

ECCL should be considered in patients with specific skin and eye lesions.

A rare case of lupus linked to thymoma shows complex diagnosis and management challenges.

A Korean baby with nevus sebaceus syndrome was found to have a KRAS gene mutation.

APS-1 in Italy shows diverse AIRE mutations and various autoimmune issues.

A 78-year-old man with Cronkhite-Canada syndrome improved significantly after treatment and remains symptom-free.

The patient with lupus and Degos' disease showed significant improvement with treatment.

Untreated congenital adrenal hyperplasia can lead to complications like stroke and needs glucocorticoid treatment.

Vogt-Koyanagi-Harada disease affects vision and skin, mainly in people with darker skin, and is treated with steroids and immunosuppressants.

Most women with ankylosing spondylitis tested positive for HLA-B27, suggesting it's useful for diagnosis.

Systemic Lupus Erythematosus has varied symptoms and is hard to diagnose, affecting many body parts and requiring careful clinical judgment.

A girl initially thought to have a psychiatric disorder was later found to have a lupus-related condition, which improved with proper treatment.