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A boy with a rare skin condition and kidney disease improved with cyclosporine after steroids failed, suggesting a new treatment approach.

A patient with Cronkhite-Canada Syndrome developed colon cancer that spread to the liver, showing the need for regular cancer checks in such patients.

Biomedical engineers are crucial for developing better treatments for chronic and autoimmune diseases.

A Brazilian male with IFAP syndrome has a unique genetic variant causing his condition.

Key genes influencing sheep hair follicle development were identified, aiding wool breeding and understanding human hair conditions.

A 37-year-old male with severe skin and internal issues has a rare inherited skin condition called dystrophic epidermolysis bullosa.

The document is a detailed medical reference on skin and genetic disorders.

The document is a detailed guide on skin conditions and treatments for dermatologists.

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

The meeting highlighted the genetic basis of female pattern hair loss and various skin health insights.

The document suggests a bacteria plays a significant role in acne rosacea and that white hair can regain color after transplant, meriting more research on reversing grey hair.

Hibiscus rosa-sinensis is used in traditional medicine and is safe in high doses, with various health benefits.

Organoid technology is advancing and entering commercial use, with applications in disease modeling, drug development, and personalized medicine.

Medicinal plants in Kurdistan have potential health benefits and need more research for drug development.

Botulinum toxin is effective for medical and cosmetic uses but requires careful handling to avoid serious side effects.

Modified laparoscopic sleeve gastrectomy effectively controls diabetes and treats obesity with minimal complications.

Nutraceuticals like Ashwagandha and Astaxanthin may help with hair loss, but supplement regulation is challenging.

Enteral supplements can improve symptoms of Cronkhite-Canada syndrome.

Pre-existing skin conditions and drug reactions are the main causes of exfoliative erythroderma.

Early diagnosis and treatment with corticosteroids can improve outcomes in Cronkhite–Canada syndrome.

PCOS is a hereditary disorder that can lead to diabetes and heart disease if not treated early.

Focal palmoplantar callosities may help diagnose non-Herlitz junctional epidermolysis bullosa.

A 15-year-old girl has a skin condition causing blisters on her feet, likely inherited from her family.

The new omeprazole nanoemulgel shows promise as a topical treatment for infections.

Proteins with added sugars are crucial for plant root hair growth.

A genetic defect in vitamin D receptors causes severe rickets and hair loss in children, but some heal as they age.

Alopecia Areata affects 2% globally, with treatments like essential oils, garlic, and JAK inhibitors showing promise, but more research is needed.

Targeting endolysosomes may help treat COVID-19.

Certain genetic variations in IL18 may increase the risk of alopecia areata in Koreans.