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Hidradenitis suppurativa is caused by genetic factors, inflammation, bacteria, hormones, and lifestyle factors like obesity and smoking.

Trichoscopy is a quick and easy way to diagnose most genetic hair problems without invasive methods.

The document concludes that managing non-classical congenital adrenal hyperplasia in females requires personalized treatment, genetic counseling, and a team of specialists.

Women with nonclassical congenital adrenal hyperplasia may have a higher risk of fertility issues and miscarriages, and should get genetic counseling.

CRISPR/Cas9 gene-editing shows promise for improving sheep and goat breeding but faces challenges with efficiency and accuracy.

Genetic testing is crucial for diagnosing congenital atrichia, a rare condition causing irreversible hair loss.

New gene discoveries have improved diagnosis and treatment for skin and hair disorders, but more research is needed to fully understand them.

The meeting highlighted the importance of genetic testing and multidisciplinary approaches in pediatric dermatology.

Melanoma's complexity requires personalized treatments due to key genetic mutations and tumor-initiating cells.

Goats with BSE or scrapie show varying symptoms, and using only clinical signs may not detect all scrapie cases.

Certain genetic markers linked to reproductive potential were identified by their impact on a protein's ability to bind to genes.

Certain genetic variations in OCT1 may improve insulin sensitivity with metformin in women with PCOS.

Azathioprine's effectiveness and safety require careful monitoring and more research, especially regarding its use with corticosteroids and the role of TPMT status in patients.

CAH is a genetic disorder affecting cortisol production and causing hormonal imbalances, with treatment and diagnosis varying by form and symptoms.

Antiandrogen therapy helps treat genetic hair loss.

Some people have a genetic variation that makes them less effective at breaking down drugs.

PCOS is a genetic disorder affecting women's reproductive health, with treatments focused on symptoms like insulin resistance and fertility.

Different types of skin cells have unique genetic markers that affect how likely they are to spread cancer.

Dermatoscopy and videodermatoscopy are useful for diagnosing and monitoring various skin, hair, and nail conditions.

Congenital Adrenal Hyperplasia is a genetic disorder with two forms, causing symptoms like early puberty and severe acne, but can be identified through screening and treated with glucocorticoids.

Trichoscopy is good for diagnosing and monitoring hair and scalp problems in children but needs more research for certain conditions.

Nonclassic congenital adrenal hyperplasia is a genetic disorder causing hormone imbalances, affecting fertility and requiring personalized treatment.

The lentiviral array can monitor and predict gene activity during stem cell differentiation.

JAK inhibitors may help treat Alopecia Areata but need careful monitoring due to side effects.

Hair follicles could be used to noninvasively monitor our body's internal clock and help identify risks for related diseases.

Male pattern baldness is often genetic and linked to a hormone, with treatments like finasteride and minoxidil being effective for some men.

A Chinese male with a new genetic mutation has a skin condition and severe urinary issues, with treatments having mixed success.

Low serum complement levels in SLE patients don't always match with disease flares; monitoring C3 and C4 is useful, but cell-bound complement products might better indicate disease activity.

The document concludes that inherited epidermolysis bullosa is a challenging genetic condition requiring multidisciplinary care and new treatments.

Men have worse COVID-19 outcomes than women due to genetic and hormonal differences.