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Probe detects finasteride with high selectivity and low detection limit.

New treatments like nanotechnology show promise in improving skin cancer therapy.

Follicle Stimulating Hormone is important for fertility.

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.

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.

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.

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.

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.

A man's relapsed leprosy was successfully treated with the antibiotic sparfloxacin.

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.

Memantine may slightly improve memory in people with Down syndrome, but more research is needed.

A position effect on the TRPS1 gene causes excessive hair growth in humans and mice.

Spironolactone helps regrow hair in women with hair loss.

Mutations in the hairless gene in mice affect its expression and lead to a range of developmental issues in multiple tissues.

Intense pulsed light (IPL) is an efficient and safe method for hair removal, reducing hair by about 80%.

Mutations in the KRT85 gene cause hair and nail problems.

Boys with less severe EDA mutations in XLHED have milder symptoms and better sweat and hair production.

Certain leukemia drugs can cause severe skin reactions that may require stopping treatment.

The research concluded that selection significantly shaped the genetic variation of the X chromosome, with certain regions affected by past selective events.

Pulsed-intense light can significantly reduce hair, with effectiveness depending on treatment number and timing, and has mild side effects.

Advancements in male reproductive medicine are ongoing, but more research and improved treatments are needed in several areas.

The document concludes that over 500 genes are linked to hair disorders and this knowledge is important for creating new treatments.

A new mutation in the HR gene causes hair loss in a specific family.

Certain genetic variants in the androgen receptor are linked to higher PSA levels, potentially affecting prostate cancer screening outcomes.

Blocking DGAT1 reduces oil gland size in mice and dogs, but only mice experience hair loss.

Men have worse COVID-19 outcomes than women due to genetic and hormonal differences.

A woman's chronic head pain after hair transplant surgery was cured by removing a post-traumatic neuroma.

Environmental factors like smoking, UV exposure, and poor diet contribute to hair loss and graying, and lifestyle changes can help manage it.