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

1α,25-dihydroxyvitamin D3 directly affects cartilage growth and development.

Trichoscopy helps diagnose and treat dissecting cellulitis early, preventing scarring.

Blocking certain pathways with kinase inhibitors may help treat cutaneous lupus erythematosus.

Patients with Discoid Lupus Erythematosus have lower vitamin D and antioxidant levels and higher oxidative stress.

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

Most spinal cord injury patients in Korea experience skin problems, especially fungal infections and eczema, affecting their quality of life.

Discoid lupus erythematosus involves immune activation and fibrosis around hair follicles, with shared pathways across humans, dogs, and mice, suggesting potential treatments for both humans and animals.

The patient with both scarring and non-scarring hair loss showed complex immune reactions and improved with steroid treatment.

RCVS should be considered in thunderclap headaches, and MRA and DSA are better for diagnosis than CT angiogram.

EPDS and MS might share an immune-related cause.

Intralesional cidofovir may be a viable alternative treatment for SCC.

CCCA is a hair loss type affecting African women, possibly caused by grooming and chemicals, with various treatments and needing more research.

A Chinese family had a child with a specific gene mutation causing vitamin D-resistant rickets, but the child improved with calcium and low-dose calcitriol.

The document suggests that severe hair loss in SLE patients may be an early sign of scalp DLE, treatable with immunosuppressive therapy.

A new genetic mutation in the CDH3 gene causes hair loss and eye problems in young people.

Pseudopelade is likely an independent disease due to its distinct features.

Recognizing CVG can help diagnose systemic amyloidosis early.

Exclamation mark hairs suggest early scalp disease, while white dots indicate it's chronic.

Dysplastic nevi have unique gene expressions, making them distinct from common melanocytic nevi.

Hair shaft changes may be linked to CCCA, but their role is unclear.

Most patients with Central Centrifugal Cicatricial Alopecia at the reviewed institution were middle-aged Black women, often with no symptoms, and commonly treated with topical medications.

Pegylated interferon-alpha 2a can cause a rare nerve disorder, but early treatment can lead to full recovery.

Cicatricial alopecia involves scarring hair loss and can be treated with various medications.

Localized dystrophic epidermolysis bullosa (DEB) can lead to scarring alopecia, highlighting the need to recognize and address this complication.

A man had rare skin tumors with bone formation and cholesterol deposits.

Middle-aged women with dilated cardiomyopathy should be screened for antiphospholipid syndrome.

A specific gene mutation causes hair loss and potential eye issues, even if vision seems normal.

A new CDH3 gene mutation was found in a Spanish patient with sparse hair and eye issues.