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Using travoprost for glaucoma may cause extra hair growth and darker skin around the eyes, but these effects can reverse after stopping the drug.

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

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

Hair problems can be caused by genetics or the environment, and treatment should focus on the cause and reducing hair damage.

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

A new genetic mutation causes severe Leydig cell hypoplasia, affecting sexual development.

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

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

Two cases showed skin abnormalities without bone or neural defects.

Dermatologists should recognize diverse discoid lupus signs to avoid misdiagnosis.

CSC is linked to mineralocorticoid receptor damage, stress, and steroid use, with treatments including drugs and laser therapies to prevent eye damage.

Mitochondriopathy may cause eyelash loss.

Excessive blue light harms eye cells and disrupts sleep patterns.

Finasteride use during early pregnancy may cause limb deformities in babies.

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

Eyelash loss can be a sign of thyroid problems.

A new genetic mutation was found causing hair and eye issues in a boy.

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

A new severe form of monilethrix syndrome includes hair loss, scalp itching, cataracts, and distinct facial features.

Corticosteroid injections for hair loss may cause eye problems, so caution is needed.

Drug misuse can cause serious eye infections and other severe side effects.

Early diagnosis and comprehensive care are crucial for managing Focal Dermal Hypoplasia's complex symptoms.

Paraproteinemic keratopathy can show eye symptoms before other signs of disease, needing careful treatment and long-term follow-up.

Menstrual abnormalities in PCOS women may not greatly affect their metabolic and hormonal profile.

Clinicians should be aware of alternating thyroid conditions and their treatment.

The coronal approach is effective and safe for reducing eye bulging in Graves' eye disease.

Polarizing light microscopy can easily and reliably diagnose congenital keratinizing disorders like Netherton syndrome.

A young girl developed unusually long eyelashes with a hair loss condition without other health issues or medication causes.

Early diagnosis using eye tests and lab markers can improve treatment for pediatric Sjögren's syndrome.

Good preoperative assessment is crucial for safe and effective eyelid and brow cosmetic surgery.