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A woman with X-linked chronic granulomatous disease developed lupus-like skin lesions, improved with treatment, suggesting a unique skin condition in carriers.

The NIPAL4 mutation c.527C>A is common in Romanian patients with autosomal recessive congenital ichthyosis.

The four patients have a unique type of ichthyosis affecting hair follicles.

Common gene patterns may cause skin autoimmune diseases.

SLE patients experience two patterns of non-inflammatory symptoms: intermittent and persistent.

Diffuse alopecia areata involves more inflammation and higher allergy-related antibodies than patchy types.

Autoimmune-related phenomena do not affect the progression or characteristics of lichen sclerosus in women.

A boy with Oculodentodigital syndrome had a unique GJA1 gene mutation causing his symptoms.

Some people with chronic hair loss may have thyroid autoimmunity.

NKG2D+CD4+ T cells are higher in alopecia areata patients and may be involved in the disease.

Celiac disease patients often have psoriasis, dermatitis herpetiformis, and alopecia areata, but rarely vitiligo.

The man was diagnosed with Cronkhite-Canada syndrome, a rare disorder with GI polyps, skin issues, hair loss, and nail problems.

The technology can help diagnose and subtype autoimmune diseases by identifying specific autoantibodies.

Autoimmune thyroid disease raises the risk of many health issues but lowers the risk of lung cancer and allergic rhinitis.

The FDA did not approve certain drugs for prostate cancer prevention due to concerns about their effectiveness and potential risks.

Recognizing unusual symptoms in Crohn's disease is crucial for proper treatment.

Alopecia areata is linked to reduced T cell function and auto-immunity.

Abnormal T-cells from thymomas cause non-motor symptoms in some myasthenia gravis patients.

Diagnosing and managing Glucocorticoid Resistance Syndrome is complex due to genetic differences and varied symptoms.

Genetic testing can diagnose hair loss linked to DSG4 gene variants.

Systemic lupus erythematosus is a complex autoimmune disease mainly affecting women, with varied symptoms and unknown exact cause.

Managing recurrent painless thyroiditis is challenging and should be personalized based on episode frequency, severity, symptoms, and patient preferences.

PCOS patients with autoimmune thyroid disease have lower DHEAS levels.

A new DSG4 gene mutation causes hair defects in a young girl.

A young woman recovered well from rare simultaneous Hepatitis B and autoimmune hepatitis after treatment.

Allergies, especially dust mite allergy, may worsen alopecia areata, and desensitization could help reduce its severity.

Vogt-Koyanagi syndrome often leads to partial or complete blindness and responds poorly to treatment.

A woman with lupus and severe nerve damage improved with specific treatments.