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

Acta Med Port. 2024 Nov 4;37(11):813-814. doi: 10.20344/amp.21928. Epub 2024 Oct 4.

¹ Department of Neurosciences and Mental Health (Neurology). Unidade Local de Saúde de Santa Maria. Lisbon. Portugal.
² 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 Lisboa. Lisbon. Portugal.
³ Department of Neuroradiology. Unidade Local de Saúde de Santa Maria. Lisbon; Faculty of Medicine. Universidade de Lisboa. Lisbon. Portugal.
⁴ 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.

No abstract available

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

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