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Reflectance confocal microscopy is useful for diagnosing and monitoring skin diseases, but it has limitations and requires expertise for correct use.

Treating cystoid macular oedema in uveitis is difficult and risky.

PEODDN is a rare skin disorder with limited treatment options, best treated with laser therapy.

Two siblings with tinea capitis improved after treatment with ketoconazole.

CCCA can affect both genders and all ages, and it has a genetic component.

An epidermal cyst in the temporal bone can occur as a rare delayed complication after ear surgery.

A 21-year-old with lichen planopilaris was successfully treated, stopping disease progression and preventing crusts.

Hair follicle stem cells can be transplanted onto the eye using a fibrin carrier to help repair eye damage.

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

Targeting the narrowest part of the anterior chamber angle may help prevent pupil block in glaucoma.

Trichoscopy can help diagnose early congenital syphilis in newborns.

Hair changes and a high occipital hairline may help diagnose Trichorhinophalangeal Syndrome.

CTA is often mistaken for AA but doesn't respond to steroids and may require hair transplantation.

OCT can effectively diagnose different stages of hair loss non-invasively.

Skin debridement and antifungals successfully treated severe scalp infection without scarring.

Erythema nodosum linked to kerion can be treated effectively with antifungals and steroids to reduce scarring.

Tangent screens help detect visual field defects from vigabatrin.

Connexin mutations can cause various diseases like hearing loss and skin disorders.

Punctate follicular porokeratosis is a skin condition with specific features seen in hair follicles.

Skin CT can help diagnose rosacea by identifying specific skin features, but should be used with clinical signs to avoid misdiagnosis.

The symptoms described align more with Haberland syndrome, not Delleman-Oorthuys syndrome.

Stopping minoxidil and using prostaglandin analogues improved the man's eye condition.

Identifying and managing risk factors before cataract surgery is crucial to prevent complications.

Pachyonychia congenita is linked to a keratin gene on chromosome 17.

The flap effectively sealed leaks and served as a barrier, with minor complications, for anterior skull base surgery.

Long-term use of canthaxanthin may cause reversible changes in the eye, including crystal deposits and altered vision responses.

CCCA is a common, scarring hair loss in Black women that needs early detection.

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