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Organ transplant recipients have a higher risk of skin cancer over time, atopic dermatitis skin shows unusual bacterial and fungal patterns, a new tool for measuring hidradenitis suppurativa severity was created, and gene expression changes in male baldness suggest new treatments.

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

Hair loss from Alopecia Areata is caused by both genes and environment, with several treatments available but challenges in cost and relapse remain.

Disrupting natural body clocks increases the risk of developing type 2 diabetes.

NKG2D gene polymorphism doesn't affect SLE risk but may influence symptoms like rash and hair loss.

PCOS increases the risk of heart disease and type 2 diabetes in women.

Some birth control pills have a higher risk of blood clots than others.

Researchers found a new area on chromosome 2 linked to a genetic hair loss condition.

The mtDNA N haplogroup is linked to a higher risk of late-onset lupus and specific symptoms in Han Chinese women.

An 11-year-old child with total hair loss may have a genetic autoimmune disease, and the outlook for hair regrowth is not good.

Skin reactions to drugs are common and can be deadly, usually requiring stopping the drug and may be better prevented with genetic testing in the future.

A woman's vitiligo improved with tofacitinib treatment, and her skin color remained even after stopping the medication, but there are concerns about cancer risk.

Heavy metals like arsenic, cadmium, and lead can increase cancer risk and worsen outcomes.

Androgenetic alopecia in men is genetic and linked to health issues like obesity and heart disease, with treatments including minoxidil, finasteride, and hair transplants.

New genetic discoveries may lead to better treatments for alopecia areata.

People with Inflammatory Bowel Disease often lose hair due to stress, medication side effects, or lack of nutrients, and treatment depends on the specific cause.

Hair loss in men is mainly caused by hormones and genes, and while current treatments can slow it down, they can't fully stop it.

Sons of mothers with polycystic ovary syndrome (PCOS) have a higher risk of obesity and insulin resistance, possibly due to certain genes and factors passed down from their mothers.

Male and female hair loss have different genetic causes.

Genetic research may lead to better ways to predict and treat male-pattern hair loss.

Alopecia areata is an autoimmune disease causing patchy hair loss, often with other autoimmune disorders, but its exact causes are unknown.

New treatments for Alopecia Areata show promise but need to be more effective and affordable.

The research suggests that the global distribution of PCOS is likely due to historical human migration and that genes affecting PCOS may have different impacts on males and females.

Genes play a significant role in male-pattern baldness, and understanding them could lead to new treatments and insights into related health issues.

Female pattern hair loss has unclear causes, possibly involving genetics, hormones, and environment, and needs better treatments.

Genotyping for NUDT15 p.Arg139Cys can help predict thiopurine side effects in Japanese IBD patients.

The cause of alopecia areata is likely a mix of genetics, immune system issues, and environmental factors, with more research needed to understand it fully.

Scientists have found specific genes linked to different hair loss conditions, which could lead to new treatments.

MendelVar is a tool that helps identify important genes by combining GWAS data with Mendelian disease information.

Alopecia areata is an autoimmune disease with genetic links, treatable with certain medications, and can affect mental health.