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

P-cadherin is important for hair growth and health, and its problems can cause hair and skin disorders.

New gene identification techniques have improved the understanding and classification of inherited hair disorders.

New genes linked to ichthyosis were found, but there's still no cure; treatment options are improving.

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

Syphilis chancres can be atypical, and fiber implantation for baldness is risky and often fails.

Different harmful mutations in the CDH3 gene cause HJMD, but symptoms vary among individuals.

Using 5-alpha-reductase inhibitors, drugs for prostate issues and hair loss, may lead to eye abnormalities in men.

Coats' Plus is a genetic disorder with eye abnormalities, brain calcification, poor growth, bone and skin issues, and movement disorders.

A new mutation in the CDH3 gene causes hair loss and vision problems in a young girl.

Finasteride and dutasteride may cause macular abnormalities.

A 12-year-old boy with a rare genetic condition has progressive hair loss with no effective treatment.

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.

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.

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.

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.

Lithium therapy may cause skin problems like hidradenitis suppurativa and other side effects, which can improve after stopping the medication.

Visual field defects in lupus nephritis can be caused by hypertensive retinopathy, not glaucoma or medication toxicity.

Nitroxide drugs can safely and effectively treat age-related diseases like macular degeneration and cardiovascular issues.

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

Gene therapy with the Math1 gene helped regenerate balance-related cells and improve balance in mice.

KFSD is a genetic disorder causing hair loss and skin issues, with no effective treatment.

Some growth factors, while important for normal body functions, can cause diseases when not regulated properly.

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.

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.

Treat pediatric skin issues with accurate diagnosis, multidisciplinary team, and various treatment options.

Frontal fibrosing alopecia is a poorly understood condition with increasing cases and unclear treatment effectiveness.

An elderly man with skin amyloidosis and abnormal blood proteins was monitored without finding widespread disease after 18 months.