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

Intralesional cidofovir might be a good alternative treatment.

Friedreich's ataxia causes thin, weak hair with surface damage and cavities.

A rare cataract surgery complication was successfully treated with laser capsulotomy.

An Australian with rare hair loss and eye conditions had a gene linked to both, not seen together before.

Some family members had a condition with both loose hair and unique eye changes, possibly indicating a new type of ectodermal dysplasia.

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

A young man had vision loss, hair loss, and other symptoms, but tests showed mostly normal results except for slightly high protein in spinal fluid.

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

Mutations in the Vitamin D receptor gene can cause hair loss similar to mutations in the Hairless gene.

DPR can show different hair characteristics, as seen in two brothers with normal hair.

Early and accurate diagnosis of primary vitreoretinal lymphoma is crucial to prevent serious complications.

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

Hair evaluation is crucial for early diagnosis and management of ARCI, as hair loss often indicates severity.

AS-OCT is crucial for diagnosing VZV interstitial keratitis and avoiding unnecessary treatments.

Focal atrichia helps diagnose female pattern hair loss.

A patient with Rothmund-Thomson syndrome showed skin changes, hair loss, and dental defects but no cataracts or skeletal issues.

Segmented hair color changes can indicate active alopecia areata.

Reflectance confocal microscopy helped diagnose and manage a woman's hair loss without needing a biopsy.

Congenital atrichia with papular lesions causes permanent hair loss in children.

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

Alopecia areata patients have eye issues and need regular eye exams.

Acitretin effectively prevented skin cancer in a patient with late-onset Rothmund-Thomson syndrome.

Genetic testing is crucial for diagnosing congenital atrichia, a rare condition causing irreversible hair loss.

Altered retinoid metabolism in cicatricial alopecia suggests a balanced vitamin A diet may prevent the condition.

Mutations in the hairless gene cause hair loss and skin cysts in rhesus macaques.

Genetic testing confirmed a rare disorder causing hair loss and vision problems in a Saudi family, stressing its importance for diagnosis and counseling.

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

Higher CRBP1 levels are linked to more severe alopecia areata.