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The update highlights that non-classic congenital adrenal hyperplasia is common in women with excess male hormones, requires specific hormone tests for diagnosis, and has various treatment options depending on age and symptoms.

The environment around melanocyte stem cells is key for hair regeneration and color, with certain injuries affecting hair color and potential treatments for pigmentation disorders.

FPHL causes hair loss in women due to genetics and hormones; minoxidil and anti-androgens are treatments, and early intervention is advised.

A mouse gene mutation increases the risk of skin cancer.

Certain gene variations might be linked to severe acne in women but not in men.

Genetic risk for PCOS can affect children's growth, metabolism, and development from early life into adulthood.

There is no significant link between alopecia areata and the PON1 enzyme polymorphisms studied.

Researchers found a specific immune receptor in patients that causes severe skin reactions to a drug.

HSD3B1 gene variant and being overweight linked to hair loss in women with polycystic ovary syndrome.

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

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

Higher testosterone levels can increase the risk of certain diseases like type 2 diabetes in women and prostate cancer in men, but can also protect against autoimmune diseases and hair loss. It also affects body fat and bone density.

Certain gene variants are linked to a higher risk of polycystic ovary syndrome, hair loss, and obesity in women from western Saudi Arabia.

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.

Androgens can help prevent memory problems caused by apoE4.

Most patients with Porphyria Cutanea Tarda had skin blisters and were often affected by hepatitis C and alcohol abuse, with differences between familial and sporadic cases.

A complex X chromosome rearrangement can increase the risk of multiple autoimmune diseases.

Certain genetic markers can indicate higher or lower risk for systemic lupus erythematosus.

Shorter telomeres in white blood cells may increase the risk of a common type of hair loss.

Certain gene variations in the Vitamin D Receptor are linked to higher risk of female hair loss.

Certain fats in the blood are linked to an increased risk of male pattern baldness.

Vitamin D helps protect skin, PSORS1 gene's risk interval for psoriasis is expanded, hair follicles can be generated from mouse cells, and interferon-γ may cause pigmented skin lesions.

PCOS is often caused by hormonal imbalances that can lead to various health issues and may indicate a risk for future metabolic and cardiovascular problems.

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

Higher miR-34a levels and the A variant of the MIR-34A gene are linked to increased risk and severity of alopecia areata.

Certain SHBG gene variants, like rs727428, are linked to higher testosterone levels in women with PCOS.

Topical minoxidil helps treat female pattern hair loss, but more research needed for other treatments.

Researchers found two new genetic variants linked to Alzheimer's disease.

Long-term high testosterone levels can improve bone density and reduce body fat but may increase the risk of prostate cancer and high blood pressure.

Some people have a genetic variation that makes them less effective at breaking down drugs.