Search

everythinglearnresearchcommunity

for

Search:↓

Different STUB1 gene mutations cause varied symptoms in autosomal recessive ataxias.

Alopecia Areata is an autoimmune condition often starting before age 20, with varied treatment success and a need for personalized treatment plans.

Alopecia areata is likely caused by a combination of genetic factors and immune system dysfunction, and may represent different diseases with various causes.

The document concludes that ongoing research using animal models is crucial for better understanding and treating Alopecia Areata.

Alopecia areata involves immune response and gene changes affecting hair loss.

The conclusion is that in the Indian subcontinent, socioeconomic status, stress, and family structure affect the severity of alopecia areata, and its psychological impact is generally mild or moderate.

New treatments targeting T-cell pathways are needed for better alopecia areata management.

The document concludes that hair loss is complex, affects many people, has limited treatments, and requires more research on its causes and psychological impact.

Teprotumumab for thyroid eye disease commonly causes fatigue, brittle nails, dry eyes, hair loss, muscle spasms, and dry mouth, with rare serious events like blood clots.

Alopecia areata causes hair loss, has no cure, and various treatments exist.

Memantine may slightly improve memory in people with Down syndrome, but more research is needed.

Manage women's cholesterol with diet, exercise, and careful treatment choices, especially during pregnancy, PCOS, and menopause.

Corticosteroids are the most common treatment for alopecia areata, but many patients need better options.

The document concludes that alopecia areata is an unpredictable autoimmune hair loss condition with no cure, but various treatments exist that require personalized approaches.

Diagnosing alopecia areata is challenging and requires careful examination and various tests to distinguish it from other hair loss types.

Elidel combined with tretinoin is more effective for treating alopecia areata than Elidel alone.

Certain HLA class II alleles increase or decrease the risk of alopecia areata.

New method finds genetic links between Type 2 Diabetes and Prostate Cancer not seen before.

The new method found new shared genetic areas linked to both Type 2 Diabetes and Prostate Cancer.

Leptin-deficient mice, used as a model for Type 2 Diabetes, have delayed wound healing due to impaired contraction and other dysfunctional cellular responses.

Older, overweight women with children and a family history of hair loss are more likely to experience female pattern hair loss.

Type 2 diabetes does not change how metformin works in obese pregnant women, so dosage adjustments are not needed.

Targeting glucocorticoid action might help treat type-2 diabetes, but human trials are needed.

Inhibitors of 11β-HSD1 show potential for treating type 2 diabetes but require more testing for safety and effectiveness.

Oral feline interferon-omega improved symptoms in diabetic cats with gingivostomatitis.

The GNP crosslinked scaffold with antibacterial coating is effective for rapid wound healing and infection prevention.

Women with PCOS are more likely to have insulin resistance and obesity, especially those with the most severe type I PCOS.

Blocking a specific enzyme might help treat obesity and diabetes, but more research is needed to ensure it's safe.

Acanthosis nigricans is a skin condition that may indicate a higher risk for insulin resistance and type 2 diabetes, and more research is needed to understand and treat it.

AGA increased yearly, type I most common, and family history and seborrheic dermatitis often linked.