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A woman with subacute cutaneous lupus erythematosus had widespread skin symptoms triggered by medication and sunlight, which improved with specific treatments.

Toxic shock syndrome is caused by a complex interaction of bacterial toxins and the immune system, and understanding this can help improve diagnosis and treatment.

A male with aromatase deficiency improved bone health with estradiol treatment.

Marie Antoinette syndrome causes sudden hair whitening, but its exact cause is unknown.

Researchers created a new mouse model for studying Citrullinemia Type I and similar conditions, showing symptoms and treatment responses like those in humans.

Nonclassic congenital adrenal hyperplasia is a genetic disorder causing hormone imbalances, affecting fertility and requiring personalized treatment.

With careful management, people with congenital adrenal hyperplasia can have successful pregnancies and become parents.

NcoA4 may have roles beyond helping control gene activity, possibly affecting cell behavior and stability.

Mutations in certain receptors can cause diseases and offer new treatment options.

A woman had both Graham Little-Piccardi-Lassueur syndrome, causing hair loss, and complete androgen insensitivity syndrome, making her genetically male but physically female. This suggests androgens don't affect the hair loss condition.

Interferons are effective for some skin conditions and cancers, but can have side effects and need more research for optimal use.

A specific gene change plus an additional mutation in the same gene cause hereditary trichilemmal cysts.

Women with greater androgen sensitivity respond better to finasteride for hair loss.

Over 50% of women over 50 experience hair loss, with minoxidil being the only proven effective treatment.

Alopecia areata has a complex genetic basis that was not fully understood as of 2001.

Thyroid hormones and androgens affect gene expression in frog reproductive organs differently between males and females.

The PP2A-B55α protein is essential for brain and skin development in embryos.

Melatonin treatment increases a specific RNA in goat cells that boosts cashmere growth.

Testosterone significantly affects sexual desire in both men and women, but its impact on women is more complex and influenced by psychological factors.

Changes in testosterone and estrogen receptor genes can affect how men age, influencing body fat, hair patterns, and possibly leading to skin disorders.

A mutation in the FAM83G gene is linked to skin and hair abnormalities in two related individuals.

Women with myotonic dystrophy might get diseases related to male hormones because their body tissues are extra sensitive to these hormones.

Sardinians were historically short due to a mix of genetics and factors like disease and poor nutrition, but recent height increases suggest better living conditions had a bigger impact.

Certain gene variations might help protect against insulin resistance and glucose intolerance in people with Polycystic Ovary Syndrome.

Chemical exposure may contribute to the rise in atopic diseases and needs more research.

Androgens contribute to common male hair loss; more research needed for hair growth medication.

A woman with acne and baldness was found to have a rare ovarian condition but successfully had a child through fertility treatment.

5α-reductase inhibitors can interfere with doping tests by masking banned substances.

The unique coat of lykoi cats is likely caused by new variants in the Hairless gene.

A Taiwanese patient had hair loss and skin bumps without the usual gene mutation, suggesting other genetic factors might be involved.