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Chrysin makes docetaxel more effective and reduces its side effects in lung cancer treatment.

Patients who have hair restoration surgery at different clinics are more likely to experience increased sensitivity after surgery.

Using minoxidil for hair loss might rarely cause a vision problem where fluid builds up under the retina.

A low dose of rapamycin increases inner ear hair cell creation by boosting SOX2+ cell numbers.

Minoxidil may cause vision problems.

Spironolactone helps reduce fluid in the eye in Central Serous Chorioretinopathy, but doesn't improve vision and recurrence is common.

Low zinc levels in chronic liver disease patients are linked to more severe symptoms like taste issues and skin problems, and zinc supplements might help.

No single treatment is clearly effective for central serous chorioretinopathy.

Zebrafish need MYC and FGF to regenerate inner ear hair cells.

Using superficial temporal fascia helps prevent Frey syndrome after parotid surgery.

Pili torti is a rare condition where hair is twisted and breaks easily, often linked to genetic disorders or other health issues.

A genetic mutation in the DCAF17 gene caused Woodhouse-Sakati syndrome in a Chinese patient from a related family.

The method effectively mimics shaving damage on skin for testing skincare products.

Bioprinting could greatly improve health outcomes but faces challenges like material choice and ensuring long-term survival of printed tissues.

A woman lost vision in one eye after a forehead injection, but prompt treatment led to partial vision recovery.

PRP generally shows better results for hair regrowth than mesotherapy, but more research is needed.

Zinc is essential for plant growth and human health, but many soils lack enough zinc, affecting crops and potentially leading to health problems.

Ultraviolet rays damage hair, smoking may cause hair loss, and good nutrition is important for hair health, but genetics mainly decide hair thickness.

A patient with steroid sulfatase deficiency had a unique hair pattern and a brain malformation not previously linked to the condition.

The UD-PrOZA program successfully diagnosed 18% of adult patients with rare diseases, often using genetic testing.

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.