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Lissencephaly with Congenital Hypothyroidism: A Case Report

Lissencephaly is a malformation of cortical development associated with deficient neuronal migration and abnormal formation of cerebral convolutions or gyri. The lissencephaly spectrum consists of agyria, pachygyria, and subcortical band heterotopia. At least 19 genes have been identified in the cau...

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Detalles Bibliográficos
Autores principales:	Sahani, Shambhu Kumar, Pathak, Anil, Nepali, Bishal, Rai, Nilshan
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Journal of the Nepal Medical Association 2022
Materias:	Case Report
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9795095/ https://www.ncbi.nlm.nih.gov/pubmed/36705174 http://dx.doi.org/10.31729/jnma.7893

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