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Using minoxidil for hair loss might cause sudden vision loss, so use it with caution and monitor closely.

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

Oxidative stress plays a significant role in alopecia areata, and new treatments may include JAK inhibitors and antioxidants.

A rare genetic disease causes sparse hair and early blindness due to a gene mutation.

Systemic lupus erythematosus treatment can restore vision in patients with retinal artery occlusion.

Vitiligo causes white skin patches, often starts before age 20, and is linked to other health issues.

Using a diode laser for hair removal without eye protection can cause serious eye injuries.

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

Oral Minoxidil can cause serious eye problems, but stopping it can improve vision.

The document concludes that doctors should thoroughly check postmenopausal women with sudden increased male traits for rare conditions like androgen-producing endometrial cancer.

Light therapy may improve eye conditions by stimulating cell activity and increasing oxygen availability.

A woman's shingles infection triggered her first episode of a rare neurological disorder and blood vessel inflammation.

Bariatric surgery can cause serious mineral deficiencies, requiring better patient education and monitoring.

No single treatment is clearly effective for central serous chorioretinopathy.

Progeroid mouse models show signs of early aging similar to humans, helping us understand aging better.

Tea, especially green tea, shows promise in cosmetics for skin and hair benefits but more research is needed for effective use.

The conclusion is that genetic testing is important for diagnosing and treating various genetic hair disorders.

The document concludes that more research is needed to find effective treatments for Lichen planopilaris and Frontal fibrosing alopecia.

Type 1 diabetes often occurs with other autoimmune diseases, and personalized treatment based on genetics can improve outcomes.

Alopecia areata is a chronic condition causing hair loss, with new treatments targeting the immune system showing promise.

Genetic variants in PDE6H and LPAR6 cause vision impairment and hair loss in two Pakistani brothers.

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

The ShorT method can detect and help reduce bias in medical AI by identifying shortcut learning.

An 11-year-old boy in Saudi Arabia has a rare case of hypoparathyroidism with severe brain calcifications but normal development and no known cause.

Albumin and prednisone improved symptoms in a woman with Cronkhite-Canada syndrome, revealing potential genetic causes.

Women with PCOS have thicker parafoveal areas in their retinas, but their macular blood vessel density is normal.

Sweat hypersensitivity can cause severe skin issues in horses.

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.

Satoyoshi syndrome can cause eye problems like uveitis and retinal vein issues.

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