Autor(es):
Catamo Vaz, Deise Haua da Silva ; Costa, Maria Helena da ; Buque, Helena Agostinho ; Nzwalo, Hipólito
Data: 2024
Identificador Persistente: http://hdl.handle.net/10400.1/26117
Origem: Sapientia - Universidade do Algarve
Assunto(s): MECP2; Nodding syndrome; Mycotoxins; Mozambique
Descrição
We read with great interest the manuscript by Spencer et al. [1] suggesting a possible role of Methyl-CpG-binding protein 2 (MECP2) dysregulation in the pathogenesis of Nodding syndrome (NS), a childhood onset epileptic disorder occurring exclusively in sub-Saharan Africa. The sociodemographic and phenotypic overlap of NS with MECP2 duplication syndrome, namely the age of onset interval, female predominance;