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Follicular dystrophy in immunocompromised patients may be linked to medication or viral factors and can improve with treatment changes.

Anti-SRP myopathy can be linked to systemic lupus erythematosus and may improve with specific treatment.

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

A 54-year-old man with painful skin blisters and fever was diagnosed with Sweet syndrome and successfully treated with corticosteroids.

Glucocorticoid treatment in lupus can cause oral lesions, which need early diagnosis and comprehensive care.

Digital gangrene can be an early sign of late-onset systemic lupus erythematosus.

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

Visual field defects in lupus nephritis can be caused by hypertensive retinopathy, not glaucoma or medication toxicity.

Effective treatment improved skin and overall symptoms in a lupus patient.

SCAD can indicate ANA-negative lupus, especially in women with unusual symptoms.

Early treatment of pediatric lupus-related eye issues is crucial to prevent vision loss.

Turner's syndrome may be linked to autoimmune diseases like psoriasis and alopecia areata, needing comprehensive care.

A woman with lupus and Kikuchi-Fujimoto disease improved with treatment.

A rare case links early-onset alopecia universalis and nephrotic syndrome, suggesting genetic immune issues.

Autoimmune Polyendocrine Syndromes involve specific combinations of endocrine and non-endocrine autoimmune diseases.

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

The report shows a young man with Hutchinson-Gilford Progeria Syndrome had typical and additional eye problems related to the disease.

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

Accurate diagnosis is crucial for effectively treating severe alopecia and related symptoms.

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

Tinea faciale can be mistaken for lupus due to similar symptoms.

Tofacitinib successfully treated a woman's severe symptoms from a rare autoimmune condition.

A man with Cronkhite-Canada syndrome improved significantly with immunosuppressive therapy.

Dystonia may be part of PAS-4 and linked to immune issues.

The woman was diagnosed with lichen sclerosus, a rare skin condition, after initial misdiagnosis and ineffective treatments.

Digital gangrene can be an unusual first sign of late-onset lupus.

Genetic screening is crucial for accurately diagnosing APS-1 due to its varied symptoms.

Early genetic testing and JAK inhibitors can help treat systemic inflammation in SAVI patients.

SLE symptoms in Dubai are similar to those in other Arab and Western countries.

A man with Isaac's syndrome affecting only one side of his body improved after immune system-targeted treatment.