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A 13-year-old boy with a rare scalp condition improved significantly with isotretinoin, minoxidil, oral steroids, and antiseptic shampoo.

Two sisters with Netherton's syndrome had skin and hair issues, needing special diet and ointments.

A patient with granuloma annulare experienced both isotopic and isomorphic responses, with skin lesions responding to steroids but relapsing after stopping treatment.

All four treatments for early rheumatoid arthritis had similar and mostly mild side effects.

The Korean study found that twenty-nail dystrophy mainly affects adults, more often women, and has five distinct types with different clinical progressions.

Necrobiosis lipoidica may need new criteria for accurate diagnosis due to similarities with another condition.

Zinc supplements and genetic analysis help treat acrodermatitis enteropathica in children.

Nonclassic congenital adrenal hyperplasia is a genetic disorder causing hormone imbalances, affecting fertility and requiring personalized treatment.

The twins' condition is unique and doesn't match any known syndromes.

Azathioprine caused side effects in over half of the Korean pediatric inflammatory bowel disease patients, requiring close monitoring.

Thymoma-associated multiorgan autoimmunity can cause liver damage and affects multiple organs, with limited treatment options and a generally poor prognosis.

Two new mutations in the CDH3 gene cause hair loss and vision problems in a young girl.

Pre-sternal keloids are more common in males and can be effectively treated with injections, though recurrences may need more treatment.

Patients with central centrifugal cicatricial alopecia often have higher rates of metabolic, autoimmune, and atopic conditions, as well as anxiety and depression.

Dermoscopy helped diagnose a rare skin disease which slightly improved with treatment.

Age and diabetes are linked to larger trichilemmal cysts, while hypertension is linked to smaller ones.

Chitosan-coated spironolactone nano carriers effectively treat acne without side effects.

A Jordanian family with Clouston syndrome has a common GJB6 gene mutation.

A hair tightly wrapped around a toddler's toe caused severe crying and was treated by surgery.

The meeting highlighted the complexity and variability of skin conditions and differing opinions on their diagnoses and treatments.

Nails can reveal important health information about skin and body conditions.

A 30-year-old man with rare skin conditions improved with antibiotics and surgery, hinting at a link to rosacea.

New techniques and materials improve sternum reconstruction and patient quality of life.

Hidradenitis suppurativa may be more severe in people with Mediterranean fever gene mutations.

Hidradenitis Suppurativa is likely an autoinflammatory disease, and better understanding its causes could improve treatments.

The patient was diagnosed with oral lichen sclerosus and needs long-term monitoring.

The dog's back mass was a keratoacanthoma with inflammation, successfully removed without recurrence.

Mast cells and the CB1 receptor may be key in causing IgA vasculitis.

A neck lesion misdiagnosed as benign was later treated successfully with Mohs Micrographic Surgery.

Chemotherapy provides symptom relief and extends life in 30-50% of gynecological cancer cases, but has only cured choriocarcinoma.