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The boy's hair and skin color differences are due to a pigmentation disorder.

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

CDH3-related disease causes worsening eye and hair issues.

A boy had a rare scalp condition with thickened skin and different-colored hair.

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

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

Mice with LSS deficiency showed hair loss and cataracts, similar to humans, and can help in understanding and treating this condition.

Frontalis suspension surgery using autologous fascia lata is effective for treating unilateral congenital ptosis with poor levator function.

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

Gomez–Lopez–Hernandez syndrome can cause focal hair loss and developmental delays but some children can still function well and excel in school and sports.

The Sacred Heart Bilobed Flap is a surgical method for repairing small scalp defects with local flaps, relying on scalp elasticity and hair regrowth to hide any imperfections.

Biotinidase deficiency can cause vision and walking problems in children and can improve with biotin treatment.

The document suggests a rare skin condition might be caused by a genetic phenomenon.

A rare genetic disorder causes sparse hair and vision loss due to a CDH3 gene mutation.

LALPS causes non-scarring hair loss along the Blaschko line, with unique trichoscopic findings.

A rare skin condition caused scarring hair loss on the scalp.

RCM and dermoscopy help identify different types of hair loss in children.

The modified Crawford technique resulted in less lagophthalmos and better cosmetic outcomes for patients with lateral droop.

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

Experience-dependent plasticity offers rehabilitation potential for macular degeneration, partial orthokeratology slows myopia, and axis misalignment affects astigmatism surgery effectiveness.

Orbital decompression surgery for Graves' orbitopathy caused double vision in 19% of patients, with similar rates for two surgical methods.

Visual field defects in lupus nephritis can be caused by hypertensive retinopathy, not glaucoma or medication toxicity.

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

Basement membrane changes in lichen planopilaris cause scarring and permanent hair loss.

The woman was diagnosed with Vogt–Koyanagi–Harada disease and successfully treated with medication, restoring her vision and stopping headaches.

Red light therapy temporarily increased blood flow in the eye but didn't change other eye structures.

Intralesional cidofovir may be a viable treatment for conjunctival lesions in Melkersson-Rosenthal syndrome without systemic toxicity.

Kallmann syndrome can cause eye issues and other health problems, requiring various treatments.

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.

LC-OCT helps accurately diagnose different types of infant hair loss without invasive methods.