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A young woman had a rare skin reaction to a medication for her joint disease, and a combination therapy improved her condition.

Daclizumab may cause psoriasis-like skin problems in multiple sclerosis patients.

Sarcoidosis can cause scarring hair loss on the scalp, which is rare.

A 25-year-old man had an unusual case of benign skin tumors and hair loss.

Chronic scarring alopecia is common in SLE patients and needs early detection and management.

Early treatment of EPDS can improve outcomes and reduce recurrence risk.

A new syndrome, Teelwani Syndrome, combines features of two rare genetic disorders.

Relapsing polychondritis might be linked to alopecia areata due to immune system factors.

Sweet syndrome can be the only sign of hairy cell leukemia relapse.

The document concludes that treatment improved skin lesions but not scalp hair loss in two patients with Graham-Little-Piccardi-Lassueur syndrome.

Ganser syndrome may result from both organic and psychogenic factors.

Minimally invasive glaucoma surgery can effectively manage glaucoma in GAPO syndrome when other treatments fail.

A 17-year-old girl with Kartagener's syndrome also has unusual skin, hair, and nail issues.

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

Patients with ichthyosis often experience symptoms similar to psoriasis and atopic dermatitis, suggesting that targeted therapies could improve their condition.

Early recognition and multidisciplinary management of Whitaker syndrome can improve patient outcomes.

Fox Fordyce disease might be more common in prepubertal girls than thought and can be managed with treatment.

Cyclosporine-A can cause excessive hair growth, which usually stops after discontinuing the drug.

Tofacitinib improved arthritis and partially improved hair loss in a lupus patient without side effects.

A new genetic mutation in the TRPV3 gene causes Olmsted-like syndrome in a Mongolian family.

Juvenile dermatomyositis can worsen quickly and needs strong treatment.

Early diagnosis and aggressive treatment are crucial for managing SLE-related pancreatitis in children.

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

A woman in Sri Lanka was diagnosed with lupus after presenting with protein loss from the gut and other symptoms.

A novel CLDN1 mutation in a 2-month-old with NISCH showed improvement with symptom management.

Antigen presenting cells around hair follicles are crucial in SLE-related hair loss.

Sonidegib effectively treated basal cell carcinoma in a patient with lupus without worsening lupus symptoms.

Vitamin D supplements should be used cautiously in sarcoidosis patients, with regular monitoring to avoid high calcium levels.

A specific gene mutation causes Olmsted syndrome.