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Most people with alopecia areata have nail changes, which are common but don't greatly affect their quality of life.

New chemotherapy drugs cause skin side effects, but treatments like minocycline and tetracycline can help reduce them.

FoxN1 overexpression in young mice harms immune cell and skin development.

The conclusion is that accurately identifying folliculosebaceous tumors requires understanding their clinical signs and microscopic features.

A new gene mutation caused a man's rare skin condition, Schöpf-Schulz-Passarge syndrome.

Oral zinc therapy is effective for treating acrodermatitis enteropathica.

Hypothyroidism in dogs is usually caused by immune system issues or gland atrophy, affects middle-aged purebreds most, and is treatable with medication.

A 6-year-old girl with Turner syndrome also had psoriasis, alopecia areata, and trachyonychia.

Higher antigliadin antibodies are linked to more severe alopecia areata, suggesting screening for celiac disease in these patients.

The document concludes that skin and nail changes can indicate various underlying health conditions.

The visfatin GT genotype may increase the risk of Alopecia Areata.

These specific gene polymorphisms are not linked to Alopecia Areata in Egyptians.

Benign skin tumors need accurate diagnosis to ensure proper treatment.

Anorexia and bulimia lead to serious health problems and increased risk of death, requiring aggressive treatment.

Lichen Planus is a less common condition affecting skin and mucous membranes, with various types and associated risk factors, challenging to diagnose, significantly impacts life quality, and may have a risk of cancerous changes in oral lesions.

The document concludes that accurate diagnosis of ichthyosis is crucial for treatment and genetic advice, and ongoing research is needed for better therapies.

LGR5 helps maintain corneal cell characteristics and prevents unwanted changes by controlling specific cell signaling pathways.

Keratin proteins are crucial for healthy skin, but mutations can cause skin disorders with no effective treatments yet.

Patients with Bohring-Opitz syndrome and ASXL1 mutations need regular kidney ultrasounds to check for tumors.

Small molecule drugs show promise for advancing regenerative medicine but still face development challenges.

Oral valganciclovir improved a patient's skin condition caused by immunosuppression.

Gene therapy has potential as a future treatment for Hutchinson-Gilford progeria syndrome.

Potassium channel openers show promise for treating heart disease and other conditions, but more research is needed to fully understand their effects and safety.

The report described a unique case of Cronkhite-Canada syndrome with unusual polyps and an association with multiple myeloma.

The conclusion is that understanding and addressing the psychological effects of alopecia areata is important for effective treatment.

A patient with Satoyoshi syndrome improved with a treatment combining several medications, including carbamazepine and methotrexate.

A rare genetic skin condition usually affecting males was found in a 9-year-old girl.

New markers and pathways have been found in skin tumors, helping better understand and diagnose them.

Vitiligo patients often have nail problems, so checking their nails is important.

The AIRE gene variant rs2075876 is linked to a higher risk of alopecia areata in males.