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New genes found linked to balding, may help develop future treatments.

Cantú syndrome is caused by mutations in the ABCC9 gene.

Genetic counselors should be culturally skilled and aware of transgender patients' unique health risks and needs.

The document concludes that insulin resistance is key in PCOS development and early treatment is crucial to prevent complications.

L-cystine and vitamin B6 at high doses prevented hair loss in mice treated with a chemotherapy drug.

Hairless gene not strongly linked to baldness.

Kids with early graying hair often have low levels of calcium, ferritin, and vitamin D3.

Genetics, stress, and health issues can cause early hair greying, which affects self-esteem, and there's no cure, only hair dye.

Early signs of PCOS in girls, like irregular periods and polycystic ovaries, suggest a need for early diagnosis and intervention to prevent further health issues.

The study suggests that a specific gene variation and higher gene activity are linked to increased baldness in Egyptian men.

The document concludes that the fast-growing direct-to-consumer genetic testing market lacks sufficient regulation, posing risks to consumers due to questionable test quality and accuracy.

Isotretinoin's effects and side effects, like birth defects and depression, might be due to it causing cell death in various cells.

Genetic variations greatly affect individual metabolism and can impact health and disease risk.

Methionine restriction works better than betaine for treating CBS deficiency symptoms in mice.

LEF1 is essential for the development of airway glands and is regulated by the Wnt/ß-catenin pathway.

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.

Ultraviolet rays damage hair, smoking may cause hair loss, and good nutrition is important for hair health, but genetics mainly decide hair thickness.

Different people show different symptoms for genetic diseases because of how sensitive their bodies are to small changes in important factors.

Brothers of women with PCOS tend to have higher levels of a hormone called DHEAS, indicating a possible genetic link.

The man has a genetic skin condition called pachyonychia congenita.

New treatments are needed for PCOS that target its genetic, hormonal, and metabolic causes.

Genetic mutations cause various hair diseases, and whole genome sequencing may reveal more about these conditions.

The conclusion suggests that PCOS may persist due to genetic traits that, while harmful for female fertility, could have provided survival and reproductive benefits to males.

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

The document concludes that skin biopsies, genetic and environmental factors, and specific treatments are important in managing cutaneous lupus erythematosus.

The conference concluded that understanding hair and nail disorders is important, iron deficiency may be linked to hair loss, and while some treatments for skin conditions are effective, they may have risks and high costs.

Despite progress in treatment, the exact cause of Alopecia areata is still unknown.

PCOS affects women's health by increasing the risk of diabetes, heart disease, and reproductive issues.

The Rotterdam Study found risk factors for elderly diseases, links between lifestyle and genetics with health conditions, and aimed to explore new areas like DNA methylation and sensory input effects on brain function.

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