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A baby girl's hair turned straight on one side due to a neck tumor and surgery, but it returned to curly as she recovered.

A 20-year-old woman had stable Progressive Hemifacial Atrophy and Vitiligo after treatment, suggesting a possible link between the conditions.

LC-OCT can help identify lupus-related scarring hair loss by spotting unique features.

Upper eyelid hyperpigmentation can help diagnose facial lichen planus pigmentosus in patients with frontal fibrosing alopecia.

The document concludes that Syndromes of Severe Insulin Resistance are rare disorders with limited treatment options.

Erosive lichen sclerosus is a distinct subtype with specific skin features, and treatment led to complete resolution in half of the cases.

Trichoscopy is useful for diagnosing and monitoring systemic lupus erythematosus, with certain hair and scalp changes indicating more active disease.

Cryptococcoid Sweet syndrome can be linked to hydralazine use and multiple autoantibodies, requiring high clinical suspicion and more research.

A 16-year-old boy with lupus had a rare brain artery issue but fully recovered with treatment.

A 13-year-old boy had both lichen planus and vitiligo, suggesting a possible link between the two conditions.

The report described a unique case of Cronkhite-Canada syndrome with unusual polyps and an association with multiple myeloma.

A rare case of isolated trichothiodystrophy was identified, marked by brittle hair with low sulfur content.

Eye exams are crucial for kids with 13q deletion syndrome, tamoxifen can cause vision loss, Propecia may lead to cataracts, Lipoid Proteinosis causes skin bumps, and OCT is useful for diagnosing macular diseases.

Cronkhite-Canada syndrome is rare, with high mortality and cancer risk, needing more research for treatment guidelines.

Three Iranian men had reddish-brown facial pigmentation with no effective treatment.

Correct diagnosis is crucial for treating overlapping conditions like NMOSD and SLE effectively.

A woman's unique dementia was misdiagnosed, a genetic mutation increases Parkinson's risk with age, and finasteride may help with Tourette syndrome.

A girl with a rare syndrome had successful hair loss treatment with no relapse after 4 years.

A patient with both bullous lichen planus and systemic lupus erythematosus showed improvement with treatment.

Cronkhite-Canada syndrome can be diagnosed without gastrointestinal polyps if there is severe mucosal atrophy and edema.

Hair loss was the first sign of a brain-related complication in a woman with lupus, and early treatment helped her hair grow back.

The CLASI is useful but needs revision to accurately assess all cutaneous lupus erythematosus subtypes.

Early diagnosis and hormone therapy can significantly improve outcomes for post-partum pituitary insufficiency in resource-limited settings.

The girl's symptoms suggest a complex condition that's hard to diagnose despite normal test results.

Managing rare genetic diseases like osteogenesis imperfecta and Escobar syndrome is complex and requires both medical and surgical treatments.

Keratosis Follicularis Spinulosa Decalvans is a rare genetic disorder causing skin and hair issues, often inherited through the X chromosome.

Autoimmune polyglandular syndrome can cause temporary brain issues that may improve on their own.

Trichoscopy helps accurately diagnose Netherton syndrome, often mistaken for atopic dermatitis.

SLE can occur in young males and cause knee pain.

Finasteride may help reduce tic severity in male Tourette syndrome patients.