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Two different mutations in the vitamin D receptor gene cause different symptoms and responses to treatment in Lebanese patients with hereditary rickets.

Both genes and environmental factors like chemicals may contribute to the increase in hypospadias, but the exact causes are still unclear.

Fadrozole and finasteride change gene expression related to sex hormones and thyroid hormones in frog larvae development.

Chicken feather gene mutation helps understand human hair disorders.

TCDD speeds up skin barrier formation by increasing certain gene expressions.

The severity of symptoms in nonclassical congenital adrenal hyperplasia is not determined by CYP21A2 gene variations.

Early diagnosis and individualized treatment improve outcomes for Congenital Adrenal Hyperplasia.

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

The conclusion suggests that prostate cancer should be classified by castration status and that new therapies targeting androgen receptor signaling show promise.

Genomic approach finds new possible treatments for hair loss.

ERβ has potential in treating prostate cancer and neurodegenerative diseases, but human studies are needed before clinical use.

Food intake, not genetics, affects how the body processes tadalafil and finasteride.

Cyproterone acetate may cause liver cancer at high doses, but is considered safe at recommended doses for approved uses.

Diagnosing sex development disorders requires combining medical history, physical exams, imaging, lab tests, and genetic data.

Cannabinoids may help treat chronic and chemotherapy-induced neuropathic pain, but more research is needed to confirm their effectiveness and safety.

Congenital Adrenal Hyperplasia is a rare inherited disease causing hormone imbalances, affecting growth, fertility, and heart health, diagnosed through blood tests and treated with medication and lifestyle changes.

Non-classical 21 hydroxylase deficiency is an underdiagnosed cause of female hair loss and polycystic ovarian syndrome.

Genetic variations affect dutasteride treatment response for male pattern hair loss.

Genetic mutations can affect female sexual development, requiring personalized medical care.

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

Oral zinc sulphate reduces dark hair color in mice.

Using 17-hydroxyprogesterone levels to diagnose nonclassic congenital adrenal hyperplasia can result in many incorrect diagnoses.

Frontal Fibrosing Alopecia's cause is unclear, affects mainly postmenopausal women, and current treatments focus on stopping hair loss rather than regrowth.

Sebaceous glands play a key role in skin health, immunity, and various skin diseases.

Estrogen increases blood vessel growth factor production, while testosterone blocks this increase.

The conclusion is that while oral contraceptive pills are effective for PCOS-related high androgen levels, new treatments with fewer side effects are needed.

Some alopecia treatments might help treat COVID-19, but more research is needed.

Taking vitamin D might improve life for MS patients and reduce skin side effects from alemtuzumab treatment.

Frontal Fibrosing Alopecia is a type of hair loss affecting mostly older women, with no agreed best treatment.