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First Korean case of Cronkhite-Canada syndrome with colon cancer and serrated adenoma.

LGR5 helps maintain corneal cell characteristics and prevents unwanted changes by controlling specific cell signaling pathways.

Necl2 affects skin cell behavior and slows wound healing.

The case suggests a possible autoimmune link between lichen sclerosus and vitiligo.

Chronic cutaneous lupus erythematosus causes scarring, hair loss, and skin discoloration, especially on sun-exposed areas.

A rare type of skin cancer on the scalp can be mistaken for hair loss, causing delayed diagnosis and severe damage.

Hair shaft malformation contributes to Central Centrifugal Cicatricial Alopecia.

Minoxidil can cause a rare eye condition, but it was successfully treated with oral Eplerenone in one case.

The report found a new type of hair loss in African-American women that affects more areas of the scalp than previously thought.

Multiple eye conditions were studied, highlighting the importance of various imaging methods for diagnosis, the vision side effects of drugs tamoxifen and Propecia, and the usefulness of optical coherence tomography for diagnosing and monitoring macular and retinal diseases.

Corticosteroids improved symptoms in a man with Cronkhite-Canada Syndrome.

Early diagnosis and effective treatment of kerion Celsi prevent scarring and permanent hair loss.

The Bsk mutation doesn't involve keratin gene recombination and its cause is unknown.

Older patients with new retinal lesions may have cancer, and local radiation might not stop it from spreading.

A 56-year-old man was diagnosed with Cronkhite-Canada Syndrome after showing symptoms like diarrhea, weight loss, and skin changes.

A CCS patient with severe complications was successfully treated using combined therapies.

Punctate follicular porokeratosis is a skin condition with specific features seen in hair follicles.

A patient with Cronkhite-Canada syndrome improved with nutritional support and steroids, but early diagnosis is key due to high mortality.

The document lists various skin conditions and structures named "corona" that are not related to the coronavirus.

Early diagnosis and strong corticosteroids are crucial for managing lymphocytic cicatricial alopecia.

Inverted follicular keratosis on the eyelid can be cured with surgery and has a great prognosis.

Systemic mastocytosis may cause a type of hair loss called cicatricial alopecia.

A 15-year-old with KID syndrome developed a rare skin condition called PEHFN.

Topical eyedrops may cause eyelash whitening and skin lightening around the eyes.

Some families have a genetic condition where they are born with irregular scalp defects.

Inherited ichthyoses cause widespread skin scaling and thickening due to gene mutations.

LC-OCT is an effective new method for diagnosing classic lichen planopilaris.

Hair follicle stem cells from aged eyelid skin can become corneal endothelial-like cells for potential eye treatments.

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

A new mutation in the CDH3 gene causes hair loss and vision problems in a young girl.