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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.

Androgens can both increase body hair and cause scalp hair loss.

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

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

KLF4 is important for maintaining stem cells and has potential in cancer treatment and wound healing.

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.

Finasteride may improve sperm count in subfertile men with low sperm count.

The safety and effectiveness of gender-affirming treatments for children are uncertain, with potential long-term risks like infertility.

Polycystic Ovary Syndrome (PCOS) is a common condition in women that can cause metabolic, reproductive, and psychological issues, and requires lifestyle changes and medication for management.

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

K_ATP channel gene mutations are linked to heart diseases, but more research is needed to understand the connection and treatment potential.

Male pattern hair loss could hint at androgens affecting COVID-19 severity.

Targeting androgen receptors could be a promising way to treat skin disorders with fewer side effects.

The AUTS2 gene is linked to neurological disorders and may affect human brain development and cognition.

New treatments targeting specific genes show promise for treating keratin disorders.

Cholesterol sulfate buildup due to a genetic mutation disrupts the skin barrier, leading to the scaling skin seen in X-linked ichthyosis.

S5αR inhibitors might help treat schizophrenia and other mental disorders but need more research.

Alopecia areata can cause unpredictable hair loss, and treatments like corticosteroids and minoxidil may help but have varying side effects.

The document concludes that alopecia areata is an autoimmune disease without a definitive cure, but treatments like corticosteroids are commonly used.

The study found that immune responses disrupt hair growth cycles, causing hair loss in alopecia areata.

The document concludes that Nonclassic Congenital Adrenal Hyperplasia requires personalized treatment plans to manage symptoms and fertility, with glucocorticoids being a common therapy.

The conclusion is that genetic changes in the glucocorticoid receptor can lead to conditions affecting stress response, immunity, and metabolism, requiring personalized treatment.

Non-classic congenital adrenal hyperplasia is a common disorder causing symptoms like acne and infertility, and it's managed based on symptoms, not just test results. Treatment can improve fertility and reduce miscarriage risk.

Adrenal disorders can cause lasting brain and behavior issues in children.

Six new hair loss factors in men not linked to female hair loss.

Inhibiting AP1 in mice skin causes structural changes and weakens the skin barrier.

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

L-cystine and vitamin B6 at high doses prevented hair loss in mice treated with a chemotherapy drug.