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A new ARID1B gene variation causes Coffin-Siris syndrome 1 and early high myopia in a Chinese family.

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

Early treatment is crucial to prevent severe eye complications from caterpillar hair.

Corneal health relies on cell migration and cooperation with the lacrimal gland, not Bmi1+ cells, and Eda gene mutations can cause dry eye disease.

Mast cells may significantly contribute to central centrifugal cicatricial alopecia.

Latanoprost eye drops caused excessive cheek hair growth and eyelash whitening in a woman.

Patients with central centrifugal cicatricial alopecia often have higher rates of metabolic, autoimmune, and atopic conditions, as well as anxiety and depression.

Using 2% minoxidil for baldness treatment might cause vision distortion due to fluid build-up under the retina.

An 11-year-old girl with a rare skin disorder also had cornea issues and dry eye, needing careful management.

The study found no common cause for a girl's crystalline cataract and uncombable hair, suggesting their co-occurrence might be coincidental.

CCCA is a common, progressive hair loss condition that may not always be linked to hair care practices and requires a biopsy for diagnosis.

Researchers found a white halo around hair in most patients with a specific type of hair loss, which helps in early diagnosis and treatment.

Postmenopausal women may experience frontal hairline and eyebrow loss due to cicatricial fibrosis.

CCCA is a common hair loss condition in African American women, often inherited and influenced by hairstyling, with unique scalp features detectable by special tools.

Two new mutations in the CDH3 gene cause hair loss and vision problems in a young girl.

CCCA involves immune response and metabolism issues, suggesting new treatment options.

Oral Minoxidil can cause serious eye problems, but stopping it can improve vision.

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

Minoxidil may help prevent capsular opacification after cataract surgery.

CCCA may be caused by both hair traction and an immune response.

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

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

Murine cytomegalovirus does not cause alopecia areata in these mice.

CCCA is a scarring hair loss condition mainly in African descent women, possibly caused by genetics and hairstyling, treated with gentle hair care and medications.

Latanoprost eye drops caused excessive hair growth and eyelash whitening in a woman.

CDH3-related disease causes worsening eye and hair issues.

CCCA and lichen planopilaris have similar histological features, making them hard to distinguish.

Pimozide treatment resolved cysts and partially restored cheek fat in a man with Barraquer–Simons syndrome.

A specific gene mutation causes hair loss and potential eye issues, even if vision seems normal.