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Genetic testing for cancer risk can lead to early and life-saving treatments in people without symptoms.

Deleting TNFα gene reduces skin cancer risk in certain mice.

A genetic test can identify people at risk of male pattern baldness early, allowing for quicker treatment.

The DQB1*03 allele is linked to higher alopecia areata risk in Italians.

The A allele of the C2 gene increases the risk of lupus, while the G allele may protect against it.

The rs231775 genetic variant is linked to a higher risk and severity of Alopecia Areata in males.

Certain mutations in the PADI3 gene may increase the risk of developing a type of scarring hair loss common in women of African descent.

Hutchinson-Gilford Progeria Syndrome is a rare genetic disorder caused by a specific gene mutation, characterized by aging symptoms and managed by monitoring heart health and using low-dose aspirin.

5α reductase type 2 enzyme mutation and oxidative stress may increase androgenetic alopecia risk in Egyptians.

Skin diseases like psoriasis, lupus, and others can increase heart disease risk due to factors like chronic inflammation and genetic susceptibility.

The rs6152 allele is not a good marker for baldness in the Indonesian population, but family history, age, gender, high blood pressure, and body weight are linked to the risk.

Androgenetic alopecia is linked to a higher risk of coronary heart disease due to certain genetic factors and high homocysteine levels.

Mutations in the WNT10A gene cause Short Anagen Hair syndrome and increase the risk of male pattern hair loss.

The book provides updated knowledge on hair disorders and new treatments for hair loss.

Genetics, nutrition, lifestyle, and hormones affect early grey hair, but more research is needed.

Insulin resistance increases the risk of developing type 2 diabetes and other health issues.

Women with nonclassical congenital adrenal hyperplasia may have a higher risk of fertility issues and miscarriages, and should get genetic counseling.

Certain genetic mutations can lower bad cholesterol and reduce heart disease risk, leading to effective cholesterol-lowering drugs.

Certain genetic variations in the SHBG gene are linked to an increased or decreased risk of PCOS in Mediterranean women.

People with hypohidrotic ectodermal dysplasia are more likely to experience long-term fatigue and hair loss after COVID-19.

Melanoma risk tools need improvement, certain gene mutations cause skin diseases and could be treated by targeting those mutations, skin wrinkling may relate to lung aging due to genetic factors, and oxidative stress affects hair loss but can be reduced in low oxygen.

PCOS may increase the risk of certain cancers.

A certain genetic variant in the androgen receptor may predict the severity of COVID-19 in men.

Oral contraceptives lower testosterone levels in women, especially those with certain genetic traits, and may be linked to increased breast cancer risk.

Balding people may have higher heart disease risk.

A specific gene change plus an additional mutation in the same gene cause hereditary trichilemmal cysts.

Premature graying of hair is linked to various health issues and can sometimes be reversed by treating underlying conditions.

Finasteride and dutasteride may help prevent hair loss but could cause side effects like sexual dysfunction and psychological issues.

The document concludes that the risk of sexual side effects from 5-alpha-reductase inhibitors is low and often temporary, but more research is needed on potential permanent effects.

A woman's unique dementia was misdiagnosed, a genetic mutation increases Parkinson's risk with age, and finasteride may help with Tourette syndrome.