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A specific gene mutation causes hair loss and potential eye issues, even if vision seems normal.

A boy with progeria had eye problems and signs of aging like hair loss and skin wrinkling.

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.

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

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 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 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.

Taking Propecia might lead to the development of cataracts.

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.

Minoxidil, a common alopecia medication, might cause eye changes due to its properties and lack of tissue selectivity.

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

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 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.

A girl with a rare syndrome had successful hair loss treatment with no relapse after 4 years.

Prompt treatment of intraocular foreign bodies is crucial to prevent blindness and improve outcomes.

VKHD and sarcoidosis may share a common cause.

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

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

Early diagnosis and treatment with Leuprolide are key for children with precocious puberty.

Over half of the diabetes patients had skin issues, with fungal infections being most common.

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

The Rotterdam Study aims to understand disease causes in the elderly and has found new risk factors and genetic influences on various conditions.

Women with PCOS have distinct retinal changes compared to healthy women.

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

Vogt-Koyanagi-Harada disease can develop during interferon therapy for chronic hepatitis C.

Injecting minced fat into the facial artery can cause severe eye problems and death, more so than other fat types, and larger amounts increase these risks.

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

Crohn's disease can cause hair loss before other symptoms appear.

Lupus can cause unusual vision problems, so it's important to consider it in such cases.

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