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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 woman's excessive hair growth and masculine features were due to a rare benign ovarian tumor and endometrial cancer, which improved after surgery.

Early and proper treatment is crucial for children with allergic conjunctivitis to avoid complications.

A patient produced cortisol after adrenalectomy, possibly due to residual tissue or other body parts making steroids.

Patients with Bohring-Opitz syndrome and ASXL1 mutations need regular kidney ultrasounds to check for tumors.

Using topical prostaglandin F2α for glaucoma may cause loss of eyelash or eyebrow pigment.

Congenital Triangular Alopecia is a rare, non-scarring hair loss that can be surgically treated in females for cosmetic reasons.

Latanoprost can cause eyelash drooping as a side effect.

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 woman with lupus and severe nerve damage improved with specific treatments.

Adrenal glands delay the start of winter fur growth in mink.

Childhood ptosis can vary from a minor cosmetic issue to a serious condition and may signal other health problems.

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.

A postmenopausal woman's hair loss and excess hair growth improved after surgery for ovarian hyperthecosis.

A 30-year-old man with rare skin conditions improved with antibiotics and surgery, hinting at a link to rosacea.

Lichen planopilaris can be triggered by prolonged scalp traction and can be treated with corticosteroids.

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

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.

A sick foal with Rhodococcus equi pneumonia was successfully treated for multiple complications with targeted therapy and careful monitoring.

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.

Painful hair loss in an elderly woman was caused by giant cell arteritis, not just aging.

Both creams are equally safe, but hydrocortisone may cause more visible blood vessels.

A stray cat with severe scabies recovered after 4 weeks of treatment.

A rare genetic mutation caused unusual skin symptoms in a man with Blau syndrome.

A baby boy had two types of temporary hair loss at birth, which might be two forms of newborn hair loss combined.

Early treatment with corticosteroids improved her eye condition significantly.

Genetic testing can help diagnose skin conditions but needs more research for full effectiveness.

Adults with Tatton-Brown-Rahman syndrome may have serious heart problems and need lifelong heart monitoring.

Early diagnosis and treatment of systemic-onset juvenile idiopathic arthritis are crucial for improvement.