Elejalde syndrome - A neuroectodermal melanolysosomal disease: a case report
Background: Elejalde syndrome is a rare neuroectodermal melanolysosomal disease with an autosomal recessive heredity. Patients usually present with silvery-gray hair, neurological abormalities, diffuse skin hypopigmentation and suntanned skin color. Case Presentation: A 3 1/2-year-old boy presented...
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Format: | Book |
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Babol University of Medical Sciences,
2024-01-01T00:00:00Z.
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A1234.567 |
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