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A woman with lupus also developed a severe skin condition linked to a genetic factor.

Alopecia areata has a complex genetic basis that was not fully understood as of 2001.

Patients with certain skin symptoms and high ANA titers should be monitored for potential systemic lupus.

Lichen Planus is a less common condition affecting skin and mucous membranes, with various types and associated risk factors, challenging to diagnose, significantly impacts life quality, and may have a risk of cancerous changes in oral lesions.

Thyroid diseases may contribute to autoimmune skin diseases, and more research is needed on their relationship.

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.

Low serum complement levels in SLE patients don't always match with disease flares; monitoring C3 and C4 is useful, but cell-bound complement products might better indicate disease activity.

Taxane chemotherapy can cause skin, hair, and nail side effects, which are often under-reported and can affect patient quality of life.

The document concludes that skin biopsies, genetic and environmental factors, and specific treatments are important in managing cutaneous lupus erythematosus.

There are still challenges in diagnosing and treating chronic skin diseases, but there is hope for future improvements.

Effective treatment for hidradenitis suppurativa varies, with antibiotics commonly used and surgery as an option, but no single method is universally successful.

The document explains various skin conditions and their treatments.

Early treatment of mixed connective tissue disease is crucial to prevent severe autoimmune conditions.

A mother and son both had ulcerative colitis and alopecia, suggesting a genetic link in autoimmune disorders and successful treatment with cyclosporine.

A woman with subacute cutaneous lupus erythematosus had widespread skin symptoms triggered by medication and sunlight, which improved with specific treatments.

The conditions alopecia areata, primary sclerosing cholangitis, and ulcerative colitis may be linked by shared autoimmune and cell death mechanisms.

Lupus affects the skin in various ways, and proper skin examination is crucial for diagnosis and treatment.

Hand and forearm transplants can be successful long-term, but they come with challenges like rejection and side effects from immunosuppression.

The study concluded that testing hormone levels after stimulation is not reliable for identifying carriers of 21-hydroxylase deficiency; genetic testing is necessary.

EGCG may help treat alopecia areata by blocking certain immune responses and reducing specific harmful immune cells.

A mother and daughter with similar hair loss conditions and identical HLA types suggest a genetic link between the conditions.

A genetic marker linked to a type of hair loss was found in most patients studied.

Both HLA-B and MICA are independently linked to alopecia areata.

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

Corticosteroid therapy reduces specific immune cells and promotes hair growth in alopecia areata patients.

Alopecia areata can be transferred through stem cell transplants from affected siblings.

B2m-free HLA variants may be a new class of HLA important in immune responses and diseases.

Severe alopecia areata involves higher levels of certain immune cells, which can be normalized with betamethasone.

Certain genetic variants are linked to frontal fibrosing alopecia in Spanish patients.

Certain genes are linked to the risk of developing Alopecia Areata.