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The Spherical Skin Model improves drug and cosmetic testing by accurately mimicking human skin for efficient compound screening.

Surgical excision is the best treatment for SCC, but intralesional cidofovir might be a viable alternative.

Soft-tissue calcification is rare in systemic lupus erythematosus.

PEVIII is a promising treatment for Pseudomonas aeruginosa keratitis.

Stem and progenitor cells in the eye have different division rates and locations, affecting how they respond to injury.

Perifollicular elastolysis is poorly understood, with limited treatment options and inconsistent results.

Regular eye exams are important for detecting serious complications in lupus patients.

3D cell spheroids can help reduce scars by delivering therapeutic vesicles.

New treatments for chronic central serous chorioretinopathy show promise in preventing permanent vision loss.

A patient with steroid sulfatase deficiency had a unique hair pattern and a brain malformation not previously linked to the condition.

Visual field defects in lupus nephritis can be caused by hypertensive retinopathy, not glaucoma or medication toxicity.

The conclusion is that skin, mucous, and eye problems after Stevens-Johnson syndrome and Lyell syndrome significantly affect patients' lives, highlighting the need for comprehensive care and eye check-ups.

Mice with LSS deficiency showed hair loss and cataracts, similar to humans, and can help in understanding and treating this condition.

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

The document reports a rare case of ECCL with a new association with optic disc colobomas.

Loss of Msx2 function causes eye development issues similar to Peters anomaly.

PCL nanoscaffold-based liver spheroids are effective for drug screening and studying liver toxicity.

The girl's "dandruff" was actually harmless hair casts, not a hygiene issue.

Surgical removal of eyelid mass showed it was non-cancerous, with no recurrence after one year.

A rare skin condition was misdiagnosed as a harmless mole on a woman's eyelid.

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

Prompt treatment of intraocular foreign bodies is crucial to prevent blindness and improve outcomes.

Pincer nails are rare in lupus patients and may be managed conservatively.

Early intervention is important for limited systemic sclerosis patients due to higher pain and ulceration risks.

Intralesional steroid injections can effectively treat calcinosis and ulcers in scleroderma.

Ossification in trichilemmal cysts is more common than previously believed.

NISCH syndrome is a rare genetic disorder affecting skin and liver, with variable symptoms and limited treatment options.

A rare neck cyst in a 47-year-old man showed diverse skin cell types and was not linked to HPV.