Moyamoya syndrome associated with neurofibromatosis type 1 in a pediatric patient
Abstract: Neurofibromatosis type 1 is a multisystem genetic disease of autosomal dominant transmission that reveals important cutaneous manifestations such as café-au-lait spots, multiple neurofibromas, and ephelides in skin fold areas, as well as hamartomatous lesions in the eyes, bones, glands, an...
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| Autores principales: | , , , |
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| Formato: | Libro |
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Sociedade Brasileira de Dermatologia,
2017-12-01T00:00:00Z.
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| Acceso en línea: | Connect to this object online. |
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| Número de Clasificación: |
A1234.567 |
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| Copia 1 | Disponible |