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

Men who start balding at age 20 may have a higher chance of getting aggressive prostate cancer.

Androgens and a high-fat diet may increase the risk of severe COVID-19 in women with PCOS by upregulating certain proteins in the heart and kidneys.

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

Acute leukemias with the Philadelphia chromosome may be biphenotypic, and identifying this is important for proper treatment.

Diagnosing and managing Glucocorticoid Resistance Syndrome is complex due to genetic differences and varied symptoms.

The KRTAP36-2 gene in sheep affects wool yield.

COVID-19 may harm male reproductive health and lower testosterone levels, potentially affecting fertility and causing erectile dysfunction. More research is needed.

A 7-month-old girl with a rare skin disorder died because diagnosis was delayed.

Certain surgical methods are better than routine incision for hidradenitis suppurativa, topical clindamycin and acitretin are effective treatments, men with HS have a risk of skin cancer, HS patients are more likely to die from heart problems, and specific genetic markers are linked to treatment response.

Vitiligo is a skin condition causing white spots, more common in women, often starts before age 20, and can affect mental health.

Finasteride may cause sexual side effects like erectile dysfunction, but they are reversible and affect less than 2% of men.

Selecting specific KRTAP26-1 gene variants can improve wool quality in sheep.

Sex hormones' effects on COVID-19 are unclear and more research is needed to understand their potential as treatment.

Chromosomal microarray analysis is important for diagnosing rare genetic variations and guiding treatment.

A specific gene mutation causes congenital hair loss.

Certain genetic changes in the LSS gene cause a rare skin and hair condition.

Low testosterone levels may lead to more severe COVID-19 outcomes.

Men and women respond differently to drugs for COVID-19, high cholesterol, and diabetes, which suggests a need for personalized treatments.

Diphenyl cresyl phosphate has low toxicity but can harm the liver, kidneys, adrenal glands, and testicles at high doses.

Eye exams are crucial for kids with 13q deletion syndrome, tamoxifen can cause vision loss, Propecia may lead to cataracts, Lipoid Proteinosis causes skin bumps, and OCT is useful for diagnosing macular diseases.

A baby boy with 13q deletion syndrome had eye cancer, a woman's vision improved after stopping a breast cancer drug, a man developed cataracts from using Propecia, and a rare skin disorder called Lipoid Proteinosis was discussed. Also, a tool called OCT is useful for diagnosing macular diseases.

Taking Propecia might lead to the development of cataracts.

The document discusses various eye conditions and their treatments, including a rare eye cancer in a baby, vision loss from a cancer drug, cataracts from a baldness treatment, a rare skin disorder, and a specific type of eye disease diagnosed with a special imaging technique.

Finasteride, often used for hair loss, can potentially cause cataracts.

Multiple eye conditions were studied, highlighting the importance of various imaging methods for diagnosis, the vision side effects of drugs tamoxifen and Propecia, and the usefulness of optical coherence tomography for diagnosing and monitoring macular and retinal diseases.

An 81-year-old man's white hair began to regain its original color while he was treated with lenalidomide, suggesting that graying hair might be reversible.

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

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

There's no significant link between the D19S884 marker at the insulin receptor gene and polycystic ovary syndrome.