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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.

The document concludes that careful diagnosis is crucial for chromosome 13q deletion syndrome, tamoxifen can cause reversible eye damage, finasteride may be linked to cataracts, and OCT is useful for diagnosing macular diseases.

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.

The skin protects the body, regulates temperature, senses touch, and makes vitamin D.

Fetal death was caused by umbilical cord stricture with hair growth in the Wharton jelly.

A 19-year-old male had two rare skin conditions causing scarring and permanent hair loss.

A Saudi individual initially identified as a girl had a genetic disorder affecting gender development.

Hormonal imbalances are a key cause of missed menstrual periods in women.

People with Down syndrome have higher rates of certain immune-related conditions and need special medical attention.

Certain changes in the SHBG gene may increase the risk of PCOS in Iraqi women.

A one-year-old child with a genetic condition had symptoms improved by treating zinc deficiency.

The document is a detailed medical reference on skin and genetic disorders.

A mother and daughter have a rare genetic hair loss disorder with no effective treatment.

Different scalp and hair disorders are more common in certain ethnic groups, with the most common being androgenetic alopecia, which is treated with medications like minoxidil and finasteride.

Cancer treatments targeting specific cells often cause skin, hair, and nail problems, affecting patients' lives and requiring careful management.

Busulfan/cyclophosphamide and total bone irradiation are equally effective for AML transplants.

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

Experts agree that PCOS affects women's health in complex ways, but more research is needed to understand and treat it effectively.

The vitamin D receptor is crucial for bone health and affects various body systems, with mutations potentially leading to disease.

Male hormones may play a role in the development of heart disease, and more research is needed to understand their effects.

Epithelial-mesenchymal interactions control hair growth cycles through specific molecular signals.

PCOS is common among Chinese women of reproductive age and linked to serious metabolic and reproductive issues, especially in obese women.

Mutations in the SRD5A3 gene cause a new type of glycosylation disorder by blocking the production of a molecule necessary for protein glycosylation.

Msx and Dlx genes are crucial for development, controlling cell behaviors like growth and differentiation through their roles as gene regulators.

Creating stronger blockers for skin enzymes might lead to better treatment for conditions like acne and excessive hair growth.

Eph receptors and ephrins may be promising targets for treating diseases, but more understanding is needed for effective and safe therapies.

Men are more likely to have severe COVID-19 cases and fatalities than women due to factors like lifestyle, aging, and biological differences.

Epigenetic changes control how adult stem cells work and can lead to diseases like cancer if they go wrong.

CDP is crucial for lung and hair follicle cell development.