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Transplantation is effective for stable leucoderma but not for progressive, widespread vitiligo vulgaris.

A woman's hair turned white after taking a cancer drug called dasatinib.

Early diagnosis and treatment with corticosteroids can improve outcomes in Cronkhite–Canada syndrome.

Newborns with ichthyosis need specific care based on their skin type.

A rare genetic mutation causes resistance to vitamin D, leading to severe rickets and requiring high doses of calcium and vitamin D for treatment.

Early diagnosis and lifelong zinc supplementation are crucial for treating acrodermatitis enteropathica effectively.

Persistent papular plaques on children's faces need better understanding and treatment.

Pregnant women often experience various skin changes, with pigment changes and stretch marks being most common.

Diagnosing Sertoli-Leydig cell tumors is challenging due to their unusual symptoms and can occur at any age.

Chronic alcoholics most commonly experience skin infections.

Daclizumab may cause psoriasis-like skin problems in multiple sclerosis patients.

The child has a scaly rash and fever, but tests show no infection.

CYP11A1 is crucial for skin health and disease by producing important steroids.

Two genetic disorders affect biotin metabolism, causing severe skin, hair, and metabolic issues.

Patients with the same vitamin D receptor mutation showed different symptoms due to other factors.

Diagnosing simple-virilizing congenital adrenal hyperplasia can be difficult and requires thorough testing and expert advice.

Frequent blood transfusions in beta thalassemia patients can lead to thyroid problems.

The man was diagnosed with lupus and improved with treatment.

Protein-losing enteropathy worsened with lupus symptoms but improved with prednisolone.

A patient with a PLEC mutation has epidermolysis bullosa, muscular dystrophy, and myasthenia gravis, which improved with steroid treatment.

A woman's skin and hair conditions improved after her cancerous tumor was removed.

The woman's skin condition persisted for 20 years despite treatments.

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.

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

Genetics likely cause premature graying hair, not vitamin levels.

Using cidofovir cream for a rare skin disease can cause skin darkening.

A 44-year-old woman with Down's syndrome was diagnosed with both rheumatoid and gouty arthritis and treated with multiple medications.

Early recognition and management of gastrointestinal tuberculosis in lupus patients are crucial to prevent complications.

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