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

Genetic defects in the Wnt/PCP pathway may cause congenital yellow nail syndrome.

A new mutation in the PLEC gene causes a rare condition with skin blistering, muscle weakness, and hair loss.

Early diagnosis and treatment of frontal fibrosing alopecia are crucial to prevent permanent hair loss.

Onycholemmal horn is a rare nail tumor in elderly women, treated by surgical removal.

The boy's symptoms suggest a possible new medical condition.

Hyaluronic acid fillers and combination treatments significantly improve facial defects from autoimmune diseases and are well-tolerated.

Exosomes from stem cells help improve nerve repair in rats.

Early recognition and treatment of atypical alopecia areata in infants are crucial.

A 21-year-old male has a rare scalp condition with excessive skin folds.

Recognizing skin symptoms helps diagnose and treat frontal fibrosing alopecia.

A boy with Pachyonychia congenita has a confirmed gene mutation, highlighting the need for a local genetic database in India.

Patients with Frontal fibrosing alopecia in Morocco often have skin conditions and thyroid disorders.

Eyelash drooping is linked to eyelid function and the presence of a double eyelid in Asians, and should be considered in eyelid surgery.

A cross-bred lamb with severe skin and movement issues had ichthyosis fetalis but normal vitamin A levels.

A rare skin condition usually found near the eyes was found on a farmer's scalp.

Epidermoid cysts can be better diagnosed with ultrasound by recognizing specific features and using clinical information.

Three genes linked to the development of trichilemmal cysts were found.

A 195 bp duplication in the HOXC10 gene causes crests in domestic chickens.

Hair loss improved with treatment and successful transplant.

Robertsonian translocation can cause recurrent miscarriages.

WWP2 is crucial for tooth development in mice.

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

A new gene mutation caused a man's rare skin condition, Schöpf-Schulz-Passarge syndrome.

Erythromelanosis follicularis faciei can also affect women, though it's rare.

Most UK dental schools don't teach non-surgical facial aesthetics, but dentists have a good knowledge base to provide these services.

A 19-year-old male had two rare skin conditions causing scarring and permanent hair loss.