Muscle-eye-brain Disease and Drug-resistant Seizures: Unravelling the Phenotypic Heterogeneity of Congenital Muscular Dystrophies

D. Menon, Joseph Samuel, S. Satish, R. Menon, B. Thomas, A. Radhakrishnan
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引用次数: 1

Abstract

Muscle-Eye-Brain Disease (MEB) constitutes part of a spectrum of closely overlapping Congenital Muscular Dystrophies (CMD) and neuronal migration disorders. Here, we present a child with MEB presenting with refractory epilepsy, a rare disease and all the more, a rare presenting manifestation. We hereby highlight the rarity of the syndrome per say, its presentation as refractory seizures to an Epileptologist and the radiological characteristics which help diagnosing MEB accurately obviating the need for an invasive procedure like muscle biopsy and molecular genetic studies in centres with limited infrastructure.
肌眼脑疾病和耐药癫痫:揭示先天性肌营养不良症的表型异质性
肌-眼-脑疾病(MEB)是先天性肌营养不良症(CMD)和神经元迁移障碍密切重叠的谱系的一部分。在这里,我们提出一个儿童MEB顽固性癫痫,一种罕见的疾病,更罕见的表现。我们在此强调该综合征的罕见性,其表现为癫痫学家的难治性癫痫发作,以及有助于准确诊断MEB的放射学特征,从而避免了在基础设施有限的中心进行肌肉活检和分子遗传学研究等侵入性手术的需要。
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