Histopathologic Findings Associated with Miller–Dieker Syndrome: An Autopsy Report

Miller–Dieker syndrome (MDS) is a rare genetic disorder characterized by congenital lissencephaly (absent or diminished cerebral gyri), facial dysmorphisms, neurodevelopmental retardation, intrauterine fetal demise, and death in early infancy or childhood. We present a case of a 4-year-old girl with...

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Detalles Bibliográficos
Autores principales: Bahmad, Hisham F., Ramesar, Lauren, Nosti, Cecilia, Anthonio, Gameli, Brathwaite, Carole, Vincentelli, Cristina, Castellano-Sánchez, Amilcar A., Poppiti, Robert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9680264/
https://www.ncbi.nlm.nih.gov/pubmed/36412589
http://dx.doi.org/10.3390/diseases10040095

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9680264/
https://www.ncbi.nlm.nih.gov/pubmed/36412589
http://dx.doi.org/10.3390/diseases10040095

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