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Sex hormones like estrogen and testosterone may affect COVID-19 severity differently in men and women, potentially influencing prevention and treatment strategies.

Rosuvastatin improves lipid levels, reduces inflammation, but worsens insulin sensitivity in men with early-onset hair loss.

Better hair loss models needed for research.

Using rodents for research shows that health problems in the womb can cause diseases later in life.

AGEs and their receptors play a significant role in hair loss by causing inflammation and oxidative stress.

Young HS patients often have other physical and mental health issues, and research on HS covers a wide range of topics including genetics, triggers, treatments, and the need for more data.

A man with testotoxicosis was fertile despite low FSH levels, suggesting high testosterone may allow sperm production without FSH.

Pregnant women with Systemic Lupus Erythematosus have a higher risk of blood clotting problems.

Environmental factors can cause mutations in skin proteins, leading to skin disorders.

Chronic scalp pain in trichodynia involves both body-wide and localized increased pain sensitivity.

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

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

The document concludes that effective acne treatment requires a personalized combination of therapies and long-term commitment, with retinoids being important for maintenance.

Recent progress has been made in understanding inherited hair and nail disorders.

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

AR/EDA2R gene linked to early-onset female hair loss, but 20p11 gene not involved.

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

Scientists now better understand the genetics of hypohidrotic ectodermal dysplasia, leading to more accurate diagnoses and potential new treatments.

A man with hypoparathyroidism had other health issues that led to a diagnosis of a rare autoimmune disorder, APS-1.

Aromatase gene variation may increase female hair loss risk.

Changing protein kinase levels in pituitary cells affects calcium flow and beta-endorphin release.

No strong genetic link to other skin conditions was found, but some genetic factors may make people more likely to get seborrheic dermatitis.

Genetic mutations that disrupt homocysteine breakdown lead to increased damage in mouse hair keratin.

PCOS may start before birth, involves metabolic issues, and can be treated with drugs like metformin and lifestyle changes.

Chinese domestic goats have unique genetic traits due to domestication and geographic isolation.

The document concludes that doctors should recognize congenital triangular alopecia to avoid unnecessary treatments, as it does not respond to steroids like alopecia areata does.

Genetics and nutritional deficiencies are key factors in premature graying of hair.

Genetic variants linked to ten skin diseases were found, showing both immune and non-immune factors play a role.

The study concluded that androstendione and DHEA are important for diagnosing high male hormone levels in women with excessive hair growth.

Different human traits like skin color and hair type vary between populations due to genetic adaptations to the environment.