Clinical and Neuroimaging Features of Peroxisomal Disorders

Neuropediatrics 2022; 53(01): 075-077
DOI: 10.1055/s-0041-1732312

Videos and Images in Neuropediatrics

Isabella Herman

¹Division of Neurology and Developmental Neuroscience, Department of Pediatrics, Baylor College of Medicine, Houston, Texas, United States

²Texas Children's Hospital, Houston, Texas, United States

³Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, United States

⁴Boys Town National Research Hospital, Omaha, Nebraska

,

Daniel G. Calame

¹Division of Neurology and Developmental Neuroscience, Department of Pediatrics, Baylor College of Medicine, Houston, Texas, United States

²Texas Children's Hospital, Houston, Texas, United States

³Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, United States

References
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2 Ferdinandusse S, Denis S, Mooyer PA. et al. Clinical and biochemical spectrum of D-bifunctional protein deficiency. Ann Neurol 2006; 59 (01) 92-104
3 Braverman NE, Raymond GV, Rizzo WB. et al. Peroxisome biogenesis disorders in the Zellweger spectrum: an overview of current diagnosis, clinical manifestations, and treatment guidelines. Mol Genet Metab 2016; 117 (03) 313-321
4 Schiller S, Rosewich H, Grünewald S, Gärtner J. Inborn errors of metabolism leading to neuronal migration defects. J Inherit Metab Dis 2020; 43 (01) 145-155
5 Klouwer FC, Berendse K, Ferdinandusse S, Wanders RJ, Engelen M, Poll-The BT. Zellweger spectrum disorders: clinical overview and management approach. Orphanet J Rare Dis 2015; 10: 151