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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.

Mutations in the NR3C1 gene cause a rare condition that affects hormone signaling and can lead to various symptoms, with dexamethasone as a treatment option.

A woman with acromegaly experienced severe hair loss from a drug called Lanreotide Autogel, which improved after stopping the treatment.

Using three different drugs together may better treat eye diseases like glaucoma and macular degeneration.

Activating TSPO helps protect the retina from damage caused by high eye pressure in glaucoma.

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.

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

Two new mutations in the CDH3 gene cause hair loss and vision problems in a young girl.

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.

A woman with a unique syndrome similar to TRPS has a genetic change near the TRPS1 gene, affecting its regulation.

A boy with chromosome 13q deletion syndrome developed eye cancer, a woman with breast cancer lost vision due to a rare side-effect of her treatment, a man's vision worsened after using a hair loss drug, and two rare disorders were discussed. Optical Coherence Tomography is useful for diagnosing and monitoring these conditions.

Cosmetics and procedures can cause eye issues, from mild discomfort to serious conditions, due to allergies, toxins, or poor care.

The skin is vital for protection, temperature control, fluid balance, immunity, and sensing, with damage affecting daily life and mental health.

Different treatments for alopecia areata have varying success rates and side effects; intralesional steroids are most effective.

Injecting hyaluronidase into the artery is effective for treating skin death and hair loss caused by hyaluronic acid fillers.

There are still challenges in diagnosing and treating chronic skin diseases, but there is hope for future improvements.

Insulin helps heal corneal wounds and nerves in diabetic mice by activating the Wnt signaling pathway.

There is not enough evidence to know if different ways of putting in eye drops for glaucoma work better than others.

The document explains the genetic causes and characteristics of inherited hair disorders.

The document emphasizes the importance of correctly identifying and classifying genetic hair disorders to help diagnose related health conditions.

No treatment reliably changes Alopecia Areata's course; reassurance and possibly a wig are recommended.

The review suggests thorough evaluation and genetic testing for proper diagnosis and treatment of Chrousos syndrome.

Choosing the right patients, using proper techniques, and having thorough knowledge are key to preventing and managing dermal filler complications.

Vogt-Koyanagi-Harada disease can develop during interferon therapy for chronic hepatitis C.

Synthetic antioxidants are effective, cheap, and stable, with some like zinc and cholecalciferol reducing child and cancer deaths, but the safety of additives like BHA, BHT, TBHQ, and PEG needs more research.

The Rotterdam Study aims to understand various diseases in older adults.

Tiger cubs fed artificial milk lacking certain amino acids developed eye problems and hair loss.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.