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

Stem cells in the eye have different roles and behaviors, helping maintain and repair the eye's surface.

A specific gene mutation causes sparse, brittle hair in a family.

Eyelash loss can be a sign of thyroid problems.

Oral minoxidil can potentially increase hair growth in people suffering from Central Centrifugal Cicatricial Alopecia.

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

Genetic variants in specific genes cause central centrifugal cicatricial alopecia.

More research is needed on CCCA in children, especially Black and Asian adolescents.

A black-skinned woman was diagnosed with Vogt-Koyanagi-Harada disease and treated with steroids and eye drops.

Minoxidil use was linked to a rare eye condition that improved after stopping the treatment.

Hair follicle stem cells can help treat eye surface issues by becoming corneal cells.

A boy with chromosome 13q deletion syndrome developed eye cancer, a woman with breast cancer lost vision due to a rare side-effect of her treatment, a man's vision worsened after using a hair loss drug, and two rare disorders were discussed. Optical Coherence Tomography is useful for diagnosing and monitoring these conditions.

Early and proper treatment is crucial for children with allergic conjunctivitis to avoid complications.

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

Overexpression of a specific receptor in mice skin causes skin thinning, early skin barrier formation, eye issues, and hair loss.

There is no standard treatment for CCCA, and practices vary widely.

The C-CAT tool helps assess and improve treatment for central centrifugal cicatricial alopecia.

CCCA mainly affects Black women and is linked to high-tension hairstyles, heating tools, chemical relaxants, and genetics.

The woman has a skin condition involving nodules, scars, and hair loss.

Targeting the protein Caveolin-1 might help treat a type of scarring hair loss called Frontal Fibrosing Alopecia.

Three related Persian cats have a rare, likely hereditary skin condition causing hair loss and poor coat quality, with limited treatment options.

Macular alopecia is a distinct, non-scarring hair loss pattern that mostly affects young Hispanic/Latinx females and often resolves on its own.

Damage to hair follicle stem cells may cause permanent hair loss and scarring in PCA.

Prostaglandin eye drops for glaucoma can rarely cause too much cheek hair growth.

A patient with Birt-Hogg-Dubé Syndrome also had choroidal melanoma, suggesting the need for careful eyelid exams in such patients.

A man developed myasthenia gravis after alopecia areata, and treatment improved his symptoms and stopped hair loss.

Mogamulizumab can cause hair loss and skin rashes.

Uveodermatological syndrome in dogs is hard to manage and can lead to blindness despite treatment.

A rare skin condition caused droopy and outward-turning eyelids in a patient.