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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.

Finasteride helps brain function in rats with liver-related brain issues.

Childhood ptosis can vary from a minor cosmetic issue to a serious condition and may signal other health problems.

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.

Finasteride raises suicide-linked aggression and stops clozapine's positive effects in schizophrenia animals.

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.

Vismodegib is effective for basal cell carcinoma but has severe side effects.

Researchers found a new ABCD1 gene mutation linked to a rare brain and nerve disorder with unusual brain changes.

Balancing treatment effectiveness with side effects is crucial for relapsed follicular non-Hodgkin's lymphoma, especially in older patients.

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

The review shows how to properly diagnose and treat the loss of eyebrow and eyelash hair.

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.

Both classical and L-type atypical BSE from cattle can infect goats with different incubation times, and tests can distinguish between the two strains.

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.

Harlequin mutant mice have hair loss due to low AIF protein levels and retroviral element activity.

The document concludes that systemic therapy is becoming more important in treating head and neck cancer, with new treatments showing promise.

The document explains the difficulty in diagnosing and treating brain diseases caused by the immune system and stresses the need for quick and accurate tests.

Adenosine helps human hair grow and prevents hair loss by targeting specific cells.

The conclusion is that effective cancer treatment often requires a combination of therapies, but must be carefully managed due to serious side effects and the risk of immunosuppression.

The document reports findings on genetic research, including ethical concerns about genome editing, improved diagnosis of mitochondrial mutations, solving inherited eye diseases, confirming gene roles in epilepsy, linking a gene to aneurysms, and identifying genes associated with age-related macular degeneration.

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

The document concluded that various dermatological treatments have different effectiveness and side effects, with some causing irritation, allergic reactions, or systemic effects.

The book provides a historical view of abortion in the U.S., critiques the pro-choice movement, and recommends including abortion in medical education.

Some drugs can cause serious side effects, like hypoglycemia from mix-ups, skin reactions, or depression, and while penicillamine may help rheumatoid arthritis more than auranofin, it has more severe side effects.

A 27-year-old with APS-1 showed improvement in symptoms after treatment.

Combining genetic and physical trait analysis improves diagnosis accuracy for monogenic diabetes.

Parry Romberg syndrome requires awareness and teamwork in primary care for proper diagnosis and management.

Uncombable hair syndrome causes frizzy hair and can affect the nervous system, eyes, and ears, often co-occurring with other hair, skin, nail, and teeth conditions, and is linked to three specific gene mutations.

Understanding normal hair growth and loss in children is key to diagnosing and treating hair disorders.