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Androgens may block hair growth signals, targeting this could treat hair loss.

Genetics play a role in acne, but how exactly they contribute is not fully understood.

Suppressing certain hormones might help prevent prostate cancer.

People with myotonic dystrophy type 1 have a higher chance of getting skin tumors, including melanoma.

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 document concludes that PCOS has a strong genetic component, but more research is needed to fully understand the specific genes involved.

Childhood ptosis can vary from a minor cosmetic issue to a serious condition and may signal other health problems.

A certain gene variant may increase the risk of polycystic ovary syndrome in Chinese women.

Hirsutism in women often indicates a hormonal imbalance and can be managed with a combination of hormonal treatments and hair removal methods.

People with myotonic dystrophy type 1 tend to develop basal cell carcinoma at a younger age but not more frequently than others.

Low birthweight and rapid weight gain after birth may increase the risk of developing polycystic ovary syndrome.

Different drugs can treat high male hormone levels in women, but they have various effects and some may harm a fetus.

The document reports findings on genetic research, including ethical concerns about genome editing, improved diagnosis of mitochondrial mutations, solving inherited eye diseases, confirming gene roles in epilepsy, linking a gene to aneurysms, and identifying genes associated with age-related macular degeneration.

Molecular diagnostics help identify genetic defects causing endocrine diseases, improving diagnosis and treatment options.

A girl with hereditary chorea, likely Huntington's disease, had her condition worsened by lupus.

A man with myotonic dystrophy type 1 had 28 skin cancers, suggesting a link between the disease and skin cancer, emphasizing the need for sun protection and regular skin checks.

Certain genetic markers, especially the MICA gene, are linked to alopecia areata.

Androgenetic alopecia is mainly caused by genetic factors and increased androgen activity, leading to hair follicle miniaturization.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

Genes and epigenetic changes are important in the development of Polycystic Ovary Syndrome.

Topical finasteride might be a good alternative for hair loss treatment with fewer side effects, but more research is needed.

A patient with a larger than usual genetic mutation had a broader range of symptoms for a muscle disease.

Myotonic dystrophy should be considered in patients with hair thinning, and genetic counseling is important.

Hair follicle sampling is a feasible method to measure FMRP and FMR1 mRNA levels in children.

Hair follicle sampling is a practical method for measuring biomarkers in children with and without Fragile X syndrome.

Women with myotonic dystrophy might get diseases related to male hormones because their body tissues are extra sensitive to these hormones.

The AUTS2 gene is linked to neurological disorders and may affect human brain development and cognition.

African American men with prostate cancer have more androgen receptor mutations, which may lead to more aggressive cancer compared to Caucasian American men.

Most hirsutism cases are due to PCOS, and treatment focuses on lowering testosterone and blocking its effects.