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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.

Taking Propecia might lead to the development of 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.

A gene called HDAC9 might be a new factor in male-pattern baldness.

Genetic data can predict male-pattern baldness with moderate accuracy, especially for early-onset cases in some European men.

A woman with acromegaloidism and normal growth hormone levels had a rare X-Tetrasomy, suggesting a need to study X-chromosome genes for their role in growth and facial development.

A genetic duplication on chromosome 5 was linked to a woman's unique combination of medical conditions.

A gene called APCDD1, which controls hair growth, is found to be faulty in a type of hair loss called hereditary hypotrichosis simplex.

Certain gene variations might be linked to severe acne in women but not in men.

The hr gene is crucial for skin and hair health, with mutations causing hair disorders.

The enzyme RDH12 plays a role in vision and retinal disease, with mutations leading to early onset visual loss and blindness, but the exact disease mechanism is unclear and there are no treatments yet.

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

Androgen receptors are key for development and health, affecting conditions like prostate cancer and male pattern baldness.

Cytokeratin 19 and cytokeratin 15 are key markers for monitoring the quality and self-renewing potential of engineered skin.

Betamethasone dipropionate reduced skin thickness, fish oil increased it, and combined treatment had no significant effect.

The research found that male pattern hair loss is mostly genetic and involves hair thinning due to hormonal effects and changes in gene expression.

S100A3 protein is crucial for hair shaft formation in mice.

A man with myotonic dystrophy type 1 had 28 skin cancers, suggesting a link between the disease and skin cancer, emphasizing the need for sun protection and regular skin checks.

Minoxidil and finasteride are effective for treating hair loss, with dutasteride showing potential but with side effects.

Hair follicle sampling is a feasible method to measure FMRP and FMR1 mRNA levels in children.

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

Genetic factors and diet significantly increase the risk of male pattern baldness.

A 15-year-old girl with no menstrual period was diagnosed with a genetic condition that makes her body unable to respond to male hormones, leading to female characteristics despite having male genetic makeup.

Certain genetic variations in the RAB5B gene are linked to a higher risk of polycystic ovary syndrome in Chinese Han women.

A girl with Denys-Drash syndrome was misdiagnosed due to biotin affecting her hormone test results.

A different gene near the hairless gene on chromosome 8p21 causes a rare hair loss condition in a German family.

Low-dose finasteride may cause fertility issues, but stopping it can improve sperm quality and lead to pregnancy.

Certain gene patterns in breast cancer are linked to how active hormone receptors are and could affect patient survival.

Nonclassic congenital adrenal hyperplasia is a common genetic disorder that can cause a range of symptoms and requires personalized treatment.

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.