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

The MTHFR C677T mutation may increase the risk of alopecia areata in the Turkish population.

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

Red blood cell folate levels are reliable indicators of long-term folate status in alopecia areata patients.

The 1298CC genotype in RA patients leads to higher methotrexate toxicity, while the 1298AA genotype results in better treatment response.

Lower adrenal hormone levels may cause hair loss in postmenopausal women, certain patterns help diagnose nail cancer, and a gene variant linked to higher skin cancer risk in kidney transplant patients suggests monitoring folate levels.

4-O-methylhonokiol from Magnolia officinalis significantly promotes hair growth.

The document concludes that managing health issues like menopause, cardiovascular risk, and hair loss is crucial for promoting longevity in aging women.

Cross-sex hormone therapy is important for managing gender dysphoria and requires careful monitoring and healthcare provider education.

The Rotterdam Study aims to understand various diseases in older adults.

Some vitamins and minerals like vitamin D and iron can help with certain types of hair loss, but more research is needed for others.

People with alopecia areata often have lower levels of vitamin D, zinc, and folate, but more research is needed to understand if supplements can help treat it.

The document concludes that mouse models are crucial for studying hair biology and that all mutant mice may have hair growth abnormalities that require detailed analysis to identify.

Using anabolic androgenic steroids can cause serious, lasting health problems in many parts of the body.

Androgens affect bone and fat cell development differently based on the cells' embryonic origin.

The document concludes that non-operative treatment for gender dysphoria is safe and effective, and hormone therapy does not increase cancer risk.

Certain genetic markers linked to reproductive potential were identified by their impact on a protein's ability to bind to genes.

Researchers found that most genes affecting drug responses are not fully covered by commercial SNP chips, suggesting the need for more comprehensive tools to optimize drug selection based on genetics.

Certain gene variants in estrogen receptors are linked to polycystic ovary syndrome, mainly affecting metabolism, in Tunisian women.

Environmental factors like diet and vitamin levels, especially Vitamin D, can affect autoimmune diseases differently, with lifestyle changes potentially improving outcomes.

Methotrexate side effects vary by race and sex.

A 23-year-old woman with Hashimoto’s thyroiditis improved significantly after a 15-month integrative treatment plan.

The document explains the difficulty in diagnosing and treating brain diseases caused by the immune system and stresses the need for quick and accurate tests.

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.

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

Certain gene variations may increase the risk and severity of alopecia areata.

Get head MRI for babies with achondroplasia early, use free immunoglobulin light chains to detect certain neurodevelopmental disorders, and video calls work for speech therapy in patients with facial anomalies.

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

Young women in West Bengal, India, with PCOS often have estrogen resistance, leptin receptor issues, folate deficiency, T2DM, and acanthosis, commonly linked to obesity.

A new genetic change in the DSC3 gene is linked to a rare condition causing hair loss and skin blisters in a child.