Search

everythinglearnresearchcommunity

for

Search:↓

Stress can cause a type of hair loss in mice lacking the CCHCR1 gene.

Dogs with dermatomyositis, especially Collies and Shetland Sheepdogs, need better treatments for their skin and muscle inflammation.

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 Rotterdam Study aims to understand disease causes in the elderly and has found new risk factors and genetic influences on various conditions.

The Rotterdam Study updated its design and objectives in 2012, providing insights into various diseases in the elderly, including skin cancer, bone health, liver disease, neurological and psychiatric conditions, and respiratory issues.

Alopecia areata is likely an autoimmune disease with unclear triggers, involving various immune cells and molecules, and currently has no cure.

Early diagnosis and individualized treatment improve outcomes for Congenital Adrenal Hyperplasia.

Keratinocytes help heal skin wounds by interacting with immune cells and producing substances that kill pathogens.

The update highlights that non-classic congenital adrenal hyperplasia is common in women with excess male hormones, requires specific hormone tests for diagnosis, and has various treatment options depending on age and symptoms.

Six new genetic regions linked to early hair loss also connect to Parkinson's disease and prostate cancer, possibly leading to new treatments.

Researchers found 15 new genetic links to skin traits in Japanese women.

Nonclassic adrenal hyperplasia is a genetic condition that can cause early puberty and fertility problems, treated with specific steroids.

A gene called HDAC9 might be a new factor in male-pattern baldness.

Mutations in the KRT85 gene cause hair and nail problems.

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.

Alopecia Areata is a complex, unpredictable autoimmune hair loss condition with limited treatment options and a significant psychological impact.

Acne is significantly influenced by genetics, and understanding its genetic basis could lead to better, targeted treatments.

Allergic reactions to blood thinners are rare but can be serious, requiring careful management and alternative treatments.

Genetic variants linked to ten skin diseases were found, showing both immune and non-immune factors play a role.

Toxic Epidermal Necrolysis is a rare, serious skin condition that can affect anyone, is more common in women, and may be linked to genetics, with a 20% mortality rate mainly due to sepsis.

Genetic research has advanced our understanding of skin diseases, but complex conditions require an integrative approach for deeper insight.

The document concludes that PCOS has a strong genetic component, but more research is needed to fully understand the specific genes involved.

Leptin affects skin and hair health and may worsen some skin conditions, but more research is needed to understand its full impact.

New treatments for hair loss are showing promise due to better understanding of genetics and the immune system.

Researchers found that most genes affecting drug responses are not fully covered by commercial SNP chips, suggesting the need for more comprehensive tools to optimize drug selection based on genetics.

Testosterone significantly affects sexual desire in both men and women, but its impact on women is more complex and influenced by psychological factors.

Researchers found two new genetic variants linked to Alzheimer's disease.

Genetic factors affect hair loss, and molecular testing may help predict, diagnose, and treat it.

Rare changes in the KRT82 gene are linked to a higher risk of Alopecia Areata.

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