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A new EDA gene mutation was found in a Chinese family with a specific skin disorder.

Dermoscopy is useful for diagnosing and monitoring discoid lupus erythematosus by showing specific skin patterns.

A woman's rare scalp condition worsened after using a specific arthritis medication, suggesting such medications can sometimes trigger or aggravate psoriasis.

A man has a common skin condition called seborrheic dermatitis, treated with special shampoos and sometimes medication.

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

A specific gene variant is linked to heart disease, increased heart muscle, curly hair, and thick skin on palms and soles.

Photodynamic therapy may not work for erythroplasia of Queyrat and could lead to invasive squamous cell carcinoma.

Cystic fibrosis can cause unusual symptoms like hair color changes, which can improve with proper treatment.

Promising treatments for EBS include anti-inflammatory drugs, antibiotics, creams, mTOR inhibitors, and gene editing, but more trials are needed.

A 12-year-old boy in rural south India had a rare skin condition causing hair loss and inability to sweat.

The dog's skin condition improved with treatment, and prevention includes keeping it dry, clean, and away from stray dogs.

Fragile hair in children is rarely linked to trichothiodystrophy (TTD).

A new gene mutation causes vitamin D resistance and rickets, treatable with calcium therapy.

Two siblings had a rare hair condition with banded hair, which doesn't need treatment.

Skin problems are common in thyroid disorders, with dry skin in hypothyroidism and warm, soft skin in hyperthyroidism.

Alopecia in patients with epidermolysis bullosa varies in severity and is often caused by skin blistering or trauma.

Certain skin rashes can indicate COVID-19 severity, with chilblains-like rashes linked to milder cases and livedoid patterns to more severe cases.

A 16-year-old girl's skin rash was likely caused by an infection and improved with topical steroids.

A new skin disease in four Labrador retrievers responded well to immunosuppressive treatment.

Recognizing erosive pustular dermatosis of the scalp is crucial to avoid misdiagnosis.

Managing multiple autoimmune diseases in one patient is very challenging.

A patient had both chronic lupus and systemic scleroderma, requiring careful treatment to manage symptoms.

Monilethrix is a genetic hair disorder causing fragile, beaded hair with no effective treatment.

Some domesticated animals have the same genetic skin diseases as humans, which can help doctors understand human genetic mutations.

Erosive pustular dermatosis of the scalp can occur about 17 weeks after starting EGFR inhibitors, and early minocycline may help manage it.

A 29-year-old woman with symptoms of both lupus and rheumatoid arthritis improved with specific medications.

Netherton syndrome causes skin and hair issues, confirmed by "bamboo hair" under dermoscopy, with no cure but managed with topical treatments.

Early diagnosis and prednisone treatment can improve outcomes in Cronkhite-Canada syndrome.

Juvenile dermatomyositis can worsen quickly and needs strong treatment.

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