Search

everythinglearnresearchcommunity

for

Search:↓

A 12-year-old boy's rare skin condition improved with topical treatments and may resolve by puberty.

Erosive pustular dermatosis is a rare skin disease that's hard to treat and affects the scalp or legs.

A child with Sweet syndrome was found to have chronic granulomatous disease and improved with treatment.

The document describes a rare case of IFAP syndrome, a genetic condition with symptoms of hair loss, light sensitivity, and scaly skin.

A rare case of severe scalp hair loss and nail issues in keratosis follicularis was observed.

Artefactual skin disorder involves self-inflicted skin lesions linked to mental health issues, needing combined medical and psychological treatment.

A man had a rare skin cancer that looked like a bald spot.

A woman with a rare autoimmune disorder had a blister on her eye and unique immune reaction, which was effectively treated with medication.

Dermal IgA deposition without symptoms is rare in Dermatitis herpetiformis risk groups.

A young tapir with a rare skin condition improved after treatment with wound cleaning, cream, and oral medication.

Cyclosporin is effective in treating dog skin diseases and has fewer side effects compared to other treatments.

Skin problems in COVID-19 patients are rare and may be due to the body's complex immune response or blood clotting issues.

The conclusion is that Erosive Pustular Dermatosis of the Scalp is a rare condition best treated with strong topical steroids and sometimes systemic treatment.

A man was diagnosed with a rare form of lupus after showing unique skin symptoms that responded well to treatment.

A 19-year-old man had a rare skin condition on one side of his face that looked like another skin disease.

The newborn was diagnosed with a rare skin disorder causing blisters, which requires careful wound care and family support.

A woman with severe hypothyroidism had a rare skin condition usually linked to a different thyroid disease.

Rituximab may be an effective treatment for Cronkhite-Canada syndrome with kidney disease.

A man with a rare lung-focused form of hypereosinophilic syndrome improved with steroid treatment.

A new mutation in the PLEC gene causes a rare condition with skin blistering, muscle weakness, and hair loss.

Some COVID-19 pneumonia patients in Veracruz, Mexico had rare skin issues like temporary hair loss linked to disease severity.

An elderly woman with cancer improved after treatment for a rare skin condition with coiled hairs.

A 72-year-old man was diagnosed with a rare skin form of Rosai-Dorfman disease after years of misdiagnosis.

A 37-year-old male with severe skin and internal issues has a rare inherited skin condition called dystrophic epidermolysis bullosa.

Chronic granulomatous disease may be linked to developing systemic lupus erythematosus.

Plasma therapy is becoming more popular for treating viral infections, skin conditions, and orthopedic issues, and is expected to grow in the healthcare market.

A boy with chromosome 13q deletion syndrome developed eye cancer, a woman with breast cancer lost vision due to a rare side-effect of her treatment, a man's vision worsened after using a hair loss drug, and two rare disorders were discussed. Optical Coherence Tomography is useful for diagnosing and monitoring these conditions.

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.

Three siblings had both Vohwinkel's disease and congenital alopecia, with no effective treatment.

Multiple eye conditions were studied, highlighting the importance of various imaging methods for diagnosis, the vision side effects of drugs tamoxifen and Propecia, and the usefulness of optical coherence tomography for diagnosing and monitoring macular and retinal diseases.