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In post-menopausal women, signs of increased male hormones should be checked for possible ovarian cancer.

A patient with a new PLEC gene mutation showed symptoms of both muscular dystrophy and myasthenia gravis, which improved with steroid treatment.

DM and AA may share a common cause.

Pilomatricoma is a rare, harmless skin lump that needs accurate diagnosis and timely treatment.

Demodex mites can cause eye problems like itching, dry eyes, and styes.

A baby girl has a hair disorder called monilethrix, causing fragile hair that may improve over time.

Treating cystoid macular oedema in uveitis is difficult and risky.

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

Using a diode laser for hair removal without eye protection can cause serious eye injuries.

Combined light therapy improves eye health and quality of life for those with meibomian gland dysfunction.

Uveal melanoma is hard to treat when it spreads, but a new drug, tebentafusp, helps patients live longer.

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

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.

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

Certain eye surgery complications can be managed effectively, especially in patients who have used specific prostate medications.

Certain medications and patient factors increase the risk of Intraoperative Floppy Iris Syndrome during cataract surgery, but with careful planning and technique adjustments, complications can be minimized.

Eyelash loss can be a sign of thyroid problems.

IFAP syndrome is a rare genetic disorder causing skin, hair, and eye issues, with limited treatment options.

Tanshinone IIA helps protect skin tissue from low oxygen damage by boosting certain cell markers.

Gore-Tex is effective for severe congenital ptosis, with the open approach better for no lid crease and the closed approach better for a preserved crease.

Alopecia can be reversed with timely steroid treatment in VKH and SO diseases.

The Oat mouse model shows mild retinal degeneration, useful for testing treatments.

A rare skin condition caused droopy and outward-turning eyelids in a patient.

Eyelid pilomatrixomas are rare, benign tumors that need accurate diagnosis for proper treatment.

Tamsulosin increases the risk of floppy iris during eye surgery.

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

Strabismus research has advanced with AI diagnostics, minimally invasive surgeries, and non-surgical treatments, led by the USA, China, and the UK.

If a child is losing a lot of eyelashes and it keeps happening, doctors should look carefully at their health history because it might be a sign of a different health problem.

Corneal health relies on cell migration and cooperation with the lacrimal gland, not Bmi1+ cells, and Eda gene mutations can cause dry eye disease.

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