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Early baldness increases prostate cancer risk, radiotherapy and surgery have similar second cancer rates, and ALA may reduce prostate cancer risk.

Lichen planopilaris in men often affects the scalp, eyebrows, arms, legs, and beard, with many having family members with hair loss.

A Japanese patient with IFAP syndrome had a severe MBTPS2 gene mutation but showed milder symptoms than previously observed cases.

More research and guidelines are needed for managing prostate cancer in people with high-risk genetic mutations.

A genetic mutation linked to longer life and less disease was found in the Amish, and a drug is being developed to replicate these benefits.

A new model uses specific blood markers to predict if children's hair loss will return.

The PER3 rs772027021 SNP may cause mild skin pigmentation changes in a new subtype of dyschromatosis universalis hereditaria.

Certain genetic markers on chromosome 20 are linked to hair loss in the Han Chinese from Yunnan.

People with atopic dermatitis are more likely to develop other skin conditions due to shared genetics and immune pathways.

Early balding may be a sign of future prostate problems.

CAG repeat numbers in the AR gene likely don't affect male pattern baldness in Korean men.

The keratin 5 mutation in a family with epidermolysis bullosa simplex was due to mosaicism, not a new mutation.

Androgenic alopecia in men is mainly linked to family history, hormonal imbalances, and metabolic issues, but can also be influenced by lifestyle habits, environmental factors, and deficiencies in certain vitamins and microelements like copper.

A higher genetic risk score increases the chance of getting benign prostatic hyperplasia and affects treatment outcomes in Han Chinese men.

EDA2R gene linked to hair loss.

Vitiligo is influenced by genetics and environment, and combining these factors can improve early detection and prevention.

Mothers with alopecia areata have a higher risk of adverse birth outcomes.

New research has found 14 genes linked to the risk of developing alopecia areata, improving understanding and treatment options.

A specific gene variant may increase the risk of developing Alopecia Areata.

Early-onset alopecia, especially with a family history, leads to worse outcomes and more related health issues.

Certain genetic variants are linked to frontal fibrosing alopecia in Spanish patients.

Genetic discoveries are leading to new treatments for alopecia areata.

Men with more vanadium in their blood and who drink less soy milk are more likely to have hair loss.

Premature greying of hair is common among young people at King Faisal University, especially females, and is linked to health issues, lifestyle, and family history.

Researchers found a gene mutation responsible for a rare hair loss condition.

Androgen receptor signaling causes early aging of cells important for hair growth by damaging their DNA.

The HSD3B1 variant increases hair loss risk in overweight women with PCOS.

Lichen Planus in siblings may be influenced by genetics and environment.

Pu-erh tea reduces hair loss risk in offspring.