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

Authors

  • Miguel Schön Department of Neurosciences and Mental Health (Neurology). Unidade Local de Saúde de Santa Maria. Lisbon.
  • Carla Bentes 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.
  • Carlos Morgado Department of Neuroradiology. Unidade Local de Saúde de Santa Maria. Lisbon; Faculty of Medicine. Universidade de Lisboa. Lisbon.
  • Miguel Oliveira Santos 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.

DOI:

https://doi.org/10.20344/amp.21928

Keywords:

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

Abstract

N/a.

Downloads

Download data is not yet available.

References

Natera-de Benito D, Muchart J, Itzep D, Ortez C, González-Quereda L, Gallano P, et al. Epilepsy in LAMA2-related muscular dystrophy: an electro-clinicoradiological characterization. Epilepsia. 2020;61:971-83. DOI: https://doi.org/10.1111/epi.16493

Jayakody H, Zarei S, Nguyen H, Dalton J, Chen K, Hudgins L, et al. Cobblestone malformation in LAMA2 congenital muscular dystrophy (MDC1A). J Neuropathol Exp Neurol. 2020;79:998-1010. DOI: https://doi.org/10.1093/jnen/nlaa062

Salvati A, Bonaventura E, Sesso G, Pasquariello R, Sicca F. Epilepsy in LAMA2-related muscular dystrophy: a systematic review of the literature. Seizure, 2021;91:425-36. DOI: https://doi.org/10.1016/j.seizure.2021.07.020

Downloads

Published

2024-10-04

How to Cite

1.
Schön M, Bentes C, Morgado C, Oliveira Santos M. Epilepsy Secondary to Occipital Cobblestone Malformation in an Adult Patient with Merosin-Deficient Congenital Muscular Dystrophy Type 1A. Acta Med Port [Internet]. 2024 Oct. 4 [cited 2024 Nov. 22];37(11):813-4. Available from: https://actamedicaportuguesa.com/revista/index.php/amp/article/view/21928

Issue

Section

Letters to the Editor