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A 20-year-old woman had stable Progressive Hemifacial Atrophy and Vitiligo after treatment, suggesting a possible link between the conditions.

A patient with a PLEC mutation has epidermolysis bullosa, muscular dystrophy, and myasthenia gravis, which improved with steroid treatment.

Using bimatoprost on one side of the face caused increased cheek hair growth in a patient.

Using bimatoprost on one side of the face caused increased cheek hair growth in a patient.

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

A specific gene mutation causes Olmsted syndrome.

Ulerythema ophryogenes causes hair thinning and inflammation, with limited treatment options.

A 10-year-old girl with hair and eyelash loss showed significant regrowth after treatment.

Oral isotretinoin temporarily improved skin symptoms in a child with IFAP syndrome.

A Japanese patient with IFAP syndrome had a severe MBTPS2 gene mutation but showed milder symptoms than previously observed cases.

Finasteride can cause muscle weakness and eye movement issues, even at low doses.

A new mutation in the MBTPS2 gene causes a mild form of IFAP syndrome.

A girl with a rare skin condition improved after one month of treatment with acitretin.

A rare genetic disease causes sparse hair and early blindness due to a gene mutation.

A 79-year-old man was diagnosed with a rare skin condition called nevus comedonicus on his eyelids.

Pembrolizumab can cause unusual eyelash growth, but it may still be worth continuing if cancer treatment is effective.

PRP shows promise for eye disease in animals but needs more research before being standard care.

A direct brow lift can effectively fix nerve damage and improve appearance after surgery.

Severe itching from shingles can cause hair loss due to rubbing.

Trichilemmal cysts can appear on children's eyelids and may be mistaken for other conditions.

Treatment with vitamin A did not improve the child's skin condition.

Surgery on a baby with a skin disorder improved eyelid position and eye health.

Acitretin moderately improved skin and eye issues but not hair loss or light sensitivity in a 3-year-old with IFAP syndrome.

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

A woman experienced fluctuating thyroid conditions and eye disease, but her symptoms improved with treatment.

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

A young man developed a rare, bilateral scalp condition after head trauma, causing hair loss but no neurological or eye issues.

Parry–Romberg Syndrome can involve the brain even without obvious symptoms, and a new diagnostic framework is suggested for early detection.

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