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A rare skin condition was found in a Labrador retriever outside North America.

The review says skin conditions with sterile pustules need more research for better treatments.

Desmoglein 3 is important for keeping hair follicle stem cells inactive and maintaining their special properties.

A 4-year-old girl was diagnosed with erythrokeratodermia variabilis after other treatments failed.

The document concludes that detailed clinical descriptions of seven family cases help understand dominant dystrophic epidermolysis bullosa's symptoms and inheritance.

A 9-year-old girl developed type 1 diabetes and alopecia after being treated for a rare kidney disease.

Dermoscopic features can help identify and differentiate types of pityriasis versicolor.

A woman with Fox-Fordyce disease had symptom relief using tretinoin cream.

A rare skin disorder, nevus comedonicus, can appear on one side of the body following Blaschko's lines.

A cat with severe skin issues improved with dexamethasone and cetirizine.

A 70-year-old woman with a rare skin condition improved after treatment with topical steroids and acitretin.

Folliculitis decalvans is a rare skin disease causing hair loss and requires personalized treatment.

Nevus psiloliparus lacks mature hair follicles but keeps other skin structures intact.

Fibroblast changes in systemic sclerosis may help understand disease severity and treatment.

A man with severe leprosy developed painless ulcers and numbness, treated successfully with multiple drugs and vitamins.

Familial dyskeratotic comedones are a rare, inherited skin condition that is hard to treat but may improve slightly with topical retinoids and urea cream.

A rare skin condition causing scarring was successfully treated with topical erythromycin and benzoyl peroxide.

A family showed a new condition with inherited hair loss and skin changes, possibly due to one genetic disorder.

The 595-nm pulsed dye laser effectively reduces symptoms of EFFC with minimal side effects.

Pityriasis rubra pilaris is a rare skin disorder with reddish-orange patches and thickened skin, needing better treatment understanding.

A patient with PPP had rare skin reactions to adalimumab, which improved after stopping smoking and continuing acitretin.

A mother and daughter had severe skin, hair, and eye issues linked to IFAP.

Razor bumps are linked to a genetic variant, misoprostol helps erythromelalgia pain, steroid ointments don't affect skin rhythms, and certain antibodies are common in localized scleroderma.

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

Papular mucinosis can cause eyebrow hair loss, but treatment can lead to regrowth.

A new medical syndrome may include skin changes, hair loss, sweating issues, bone malformations, leg swelling, and low cortisol.

A 16-year-old boy's facial condition improved with doxycycline, suggesting an immune response to hair follicle damage.

A woman had a skin reaction from a cough suppressant, dextromethorphan, which is a new cause of fixed-drug eruption.

A baby boy with 13q deletion syndrome had eye cancer, a woman's vision improved after stopping a breast cancer drug, a man developed cataracts from using Propecia, and a rare skin disorder called Lipoid Proteinosis was discussed. Also, a tool called OCT is useful for diagnosing macular diseases.

The man has a genetic skin condition called pachyonychia congenita.