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Using a perfusion system and 3D spheroid culture improves the growth of corneal cell layers for tissue engineering.

Correct diagnosis is crucial for treating overlapping conditions like NMOSD and SLE effectively.

Aged corneal cells can revert to a stem-like state to help repair tissue.

Patients with Systemic Sclerosis have much higher levels of GDF-15, which could help predict organ involvement and guide treatment.

A rare scalp condition causing hair loss improved with a specific cream.

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

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

Limbal Mesenchymal Stem Cell Secretome might help heal eye injuries by reducing inflammation and promoting tissue repair.

No single treatment is clearly effective for central serous chorioretinopathy.

CCCA is a scarring hair disorder mainly affecting people of African descent, needing better awareness and treatment.

Reflectance confocal microscopy helped tell periorificial dermatitis apart from similar skin conditions.

A woman with advanced eye cancer went into complete remission using a combination of immunotherapy and topical treatments.

The link between pemphigus and the patient's scarring hair loss is still unclear.

Two patients had a rare combination of red skin spots and white scaly skin lesions not on the genitals.

A woman with both Cronkhite-Canada syndrome and myelodysplastic syndrome improved significantly with corticosteroid treatment.

A rare skin condition caused scarring hair loss on the scalp.

A benign skin tumor grew quickly in a dialysis patient and was surgically removed.

A rare autoimmune disease caused the woman's scalp blisters and hair loss, successfully treated with medication.

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

People with alopecia areata have similar retinal structures but thicker choroidal regions compared to those without the condition.

Researchers created a new mouse model for studying scleroderma.

IRS premature desquamation is not unique to CCCA and occurs in various scarring alopecias.

A U.S. Naval fighter pilot suffered permanent vision loss in one eye due to recurrent central serous retinopathy.

A man with KID syndrome developed a rare cancer in a long-term skin infection.

A new genetic mutation was found causing hair and eye issues in a boy.

The patient has Chronic Cutaneous Lupus, a skin condition causing plaques and hair loss.

The study found that males with KFSD had severe skin and eye symptoms, while female carriers had milder symptoms.

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

Clouston's syndrome is a rare disorder affecting nails, hair, teeth, and skin, caused by a gene mutation, and currently has no treatment, only supportive care.