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A man with a rare skin condition and a new gene mutation developed high calcium levels due to his treatment.

The report described a unique case of Cronkhite-Canada syndrome with unusual polyps and an association with multiple myeloma.

Glucosylceramides are essential for healthy skin and proper wound healing.

Surgery can cause skin cysts in dogs.

Two patients with the same genetic mutation had both blistering skin and easily pulled out hair.

Oral calcitriol helped improve scleroderma and hair regrowth in a young woman.

Mutations in the TSPEAR gene cause a new form of ectodermal dysplasia affecting hair and tooth development.

Hair bulb cells can create skin-like tissues for potential skin repair.

Hair follicle bumps with stem cells might contribute to permanent hair loss by getting disconnected due to scarring.

The hair defect is due to abnormal inner root sheath keratinization.

The document suggests a rare skin condition might be caused by a genetic phenomenon.

Dermal sheath cells help heal wounds by showing both skin and connective tissue traits.

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

Skin cysts might help advance stem cell treatments to repair skin.

Silicon may affect calcium metabolism in dialysis patients, causing symptoms like skin eruptions and abnormal hair growth.

Infants with severe KID syndrome may be more prone to serious infections and need close monitoring.

A 4-year-old girl has a rare condition causing hairlessness and skin bumps, but normal teeth and sweating.

The new drug carriers show promise for better targeting and treating ovarian cancer.

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

PEA-ENL improves skin delivery and reduces inflammation without side effects.

Skin lesions in Carney complex are likely caused by a specific group of skin cells that promote pigment production due to a genetic mutation.

Corneodesmosin is crucial for skin and hair health, and its dysfunction can cause skin and hair disorders.

Older men's scalp damage increases with age and sun exposure, a baby girl in the Philippines has Schimmelpenning syndrome, and thyroid screening is advised for children with hair loss and certain risk factors.

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

A young boy with a rare skin and nail condition improved significantly with simple topical treatments.

HPH-15, a new compound, effectively reduces skin fibrosis in experiments without causing harm.

Substance P may play a role in the inflammation seen in keratosis follicularis spinulosa decalvans.

A specific gene change plus an additional mutation in the same gene cause hereditary trichilemmal cysts.