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Autoimmune skin disorders are caused by genetic and environmental factors and are treated with various medications and preventative strategies.

Certain gene variations are significantly linked to hair loss, especially in white people.

Polycystic ovary syndrome (PCOS) was first described in 1721, officially diagnosed in the 1990s, and is now known to be partly genetic and linked to insulin resistance, with increased risk of cardiovascular disease and carbohydrate metabolism issues.

Early hair loss may indicate risk of insulin resistance.

G allele of AR Stul polymorphism linked to higher hair loss risk, especially in white people.

The SNP rs6457452 is linked to a higher risk of alopecia areata in Koreans.

Mutation in hairless gene may increase hair loss risk.

Mutation in hairless gene may increase hair loss risk.

Hair loss may indicate a higher risk of heart disease and other health issues related to metabolism.

Human enzymes can detoxify harmful substances but might also increase their cancer risk.

Pediatric endocrinologists should provide early fertility counseling and preservation options to young patients at risk of infertility.

Male hormones affect COVID-19 severity and certain drugs targeting these hormones could help reduce the risk.

Testosterone therapy in transgender men can lead to hair loss, with the risk increasing over time and influenced by family history.

UK medical students lack dermatology education, liver biopsy patients with risk factors show more fibrosis, and certain fungi resist drugs due to melanin; genetics may influence female hair loss.

People with Major Depressive Disorder have a higher chance of getting Alopecia Areata, and vice versa; antidepressants may lower this risk.

Family history, especially on the mother's side, increases the risk of female pattern hair loss.

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

Genetic marker rs12558842 strongly linked to male hair loss.

Genetic factors alone might not cause pemphigus vulgaris; other factors like birth complications and puberty may trigger it.

iPSCs can help treat genetic skin disorders by creating healthy skin cells from a small biopsy.

Birt–Hogg–Dubé Syndrome requires genetic testing for accurate diagnosis due to its similarities with tuberous sclerosis.

Certain genes are linked to the risk of developing Alopecia Areata.

Alopecia Areata affects people of all ages worldwide, is likely caused by genetic and environmental factors, and can lead to stress and depression, highlighting the need for treatments that address both physical and mental health.

Melanoma risk tools need improvement, a gene mutation causes a hair disorder that might be treated by managing cell stress, a potential therapy for a skin-ear disorder involves blocking cell channels, skin wrinkling may indicate lung aging regardless of smoking, and oxidative stress might contribute to common baldness.

Premature aging increases the risk of immune problems and autoimmune diseases.

Men with genetic hair loss are more likely to have abnormal blood lipid levels, especially if the hair loss is severe.

Obesity increases the risk of developing polycystic ovary syndrome, and weight loss can improve the condition.

Obesity increases the risk of skin infections, inflammatory conditions, and melanoma, but not basal cell carcinoma.

Retinoids can prevent skin cancer in high-risk people but have side effects and require more research on dosing and effectiveness.

Connexin-26 gene mutations may increase cancer risk in KID syndrome patients.