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The article suggests that targeting specific immune pathways could help control and treat the skin disease hidradenitis suppurativa.

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

The congress showed that psychological therapy can help skin condition patients, social media affects acne stigma, education improves atopic dermatitis, and patient satisfaction in dermatology is high, especially with good doctor engagement.

A woman with a unique syndrome similar to TRPS has a genetic change near the TRPS1 gene, affecting its regulation.

Malt1 protease is essential for regulatory T cell function and could be targeted to boost antitumor immunity.

Coinheritance of BRCA2 and CYLD genes may lead to new treatment options for certain cancers.

African American men with prostate cancer have more androgen receptor mutations, which may lead to more aggressive cancer compared to Caucasian American men.

Three genes linked to the development of trichilemmal cysts were found.

A patient with myotonic dystrophy had several autoimmune disorders and thyroid cancer, suggesting a possible link between these conditions.

A patient with untreated congenital adrenal hyperplasia had large benign tumors in her adrenal glands removed, improving her symptoms.

Some Greek melanoma patients have gene mutations linked to increased cancer risk, a new color feature helps diagnose melanoma, the incidence of a skin condition in the Netherlands is rare, and a gene possibly affects male-pattern baldness.

E211 G>A gene linked to lower risk of severe prostate cancer and hair loss.

A boy with Sjogren-Larsson syndrome has skin and muscle symptoms due to a specific enzyme deficiency.

A 23-year-old woman with Hashimoto’s thyroiditis improved significantly after a 15-month integrative treatment plan.

Faulty inflammasome activation may lead to autoimmune skin diseases and could be a target for new treatments.

The lotion and shampoo effectively treated scalp seborrheic dermatitis.

Patients with RASopathies have a higher risk of autoimmune disorders and should be routinely screened.

Non-classic congenital adrenal hyperplasia (NCCAH) can mimic PCOS and requires genetic testing for proper diagnosis and treatment.

Acne is linked to inflammation and insulin resistance, and is associated with various syndromes that require different treatments.

Blond hair in Solomon Islanders is due to a unique genetic variant, not European ancestry.

Childhood obesity is rising globally due to various factors, and early prevention and healthy lifestyle changes are crucial.

Correct skin biopsy techniques are crucial to avoid misdiagnosis of skin diseases.

A new gene mutation causes female pseudohermaphroditism due to glucocorticoid resistance.

Researchers found a specific immune receptor in patients that causes severe skin reactions to a drug.

Restoring mitochondrial function in mice reversed their skin wrinkling and hair loss.

Some parents have a mild form of congenital adrenal hyperplasia without symptoms, and they usually don't need treatment.

The article explains the genetic causes and symptoms of various hair disorders and highlights the need for more research to find treatments.

Hair problems can be caused by genetics or the environment, and treatment should focus on the cause and reducing hair damage.

Three new types of a skin blistering disease were found, caused by specific gene mutations.

Eating high glycemic foods and drinking milk may worsen acne by increasing insulin and IGF-1 levels.