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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.

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

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

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 certain mutation in the fetal alpha 5-reductase gene is linked to a higher risk of late miscarriage.

FGF5 gene mutations cause unusually long eyelashes by affecting hair growth regulation.

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

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.

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

Methotrexate side effects vary by race and sex.

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.

Tacrolimus causes fewer acute rejections than cyclosporin A in kidney transplants but doesn't necessarily improve kidney function after one year; cardiovascular risks and side effects vary between the two drugs.

Men with early balding should be checked for metabolic syndrome, as there's a link between the two.

PCOS increases the risk of heart disease and type 2 diabetes in women.

Hair loss from Alopecia Areata is caused by both genes and environment, with several treatments available but challenges in cost and relapse remain.

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

Drinking a lot of alcohol increases the risk of prostate cancer and can worsen the condition.

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

Follicle Stimulating Hormone is important for fertility.

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

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

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

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.

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

Editing the FGF5 gene in sheep increases fine wool growth.

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

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

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.

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