Epilepsy Secondary to Occipital Cobblestone Malformation in an Adult Patient with Merosin-Deficient Congenital Muscular Dystrophy Type 1A.

Schön, Miguel; Bentes, Carla; Morgado, Carlos; Oliveira Santos, Miguel

Schön, Miguel; Bentes, Carla; Morgado, Carlos; Oliveira Santos, Miguel.

Afiliación

Schön M; Department of Neurosciences and Mental Health (Neurology). Unidade Local de Saúde de Santa Maria. Lisbon. Portugal.
Bentes C; Department of Neurosciences and Mental Health (Neurology). Unidade Local de Saúde de Santa Maria. Lisbon; EEG/Sleep Laboratory/Stroke Unit Department of Neurosciences and Mental Health. Unidade Local de Saúde de Santa Maria. Lisbon; Centro de Estudos Egas Moniz. Faculty of Medicine. Universidade de
Morgado C; Department of Neuroradiology. Unidade Local de Saúde de Santa Maria. Lisbon; Faculty of Medicine. Universidade de Lisboa. Lisbon. Portugal.
Oliveira Santos M; Department of Neurosciences and Mental Health (Neurology). Unidade Local de Saúde de Santa Maria. Lisbon; Centro de Estudos Egas Moniz. Faculty of Medicine. Universidade de Lisboa. Lisbon. Portugal.

Acta Med Port ; 2024 Oct 04.

Article en En | MEDLINE | ID: mdl-39366001

Palabras clave

Epilepsy/etiology; Laminin/genetics; Muscular Dystrophies/congenital; Nervous System Malformations/genetics

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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Acta Med Port Año: 2024 Tipo del documento: Article Pais de publicación: Portugal

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