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MRI findings of hypomyelination in adenylosuccinate lyase deficiency

Adenylosuccinate lyase deficiency is a rare genetic disorder with few reported cases in the United States. Magnetic resonance imaging findings in the brain include hypomyelination and low generalized parenchymal volume. Presented here is a case in a 3-month-old male who presented with hypotonia and...

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Detalles Bibliográficos
Autores principales: Kayfan, Samar, Yazdani, Rana M., Castillo, Samantha, Wong, Kevin, Miller, Jeffrey H., Pfeifer, Cory M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6260459/
https://www.ncbi.nlm.nih.gov/pubmed/30510607
http://dx.doi.org/10.1016/j.radcr.2018.11.001
Descripción
Sumario:Adenylosuccinate lyase deficiency is a rare genetic disorder with few reported cases in the United States. Magnetic resonance imaging findings in the brain include hypomyelination and low generalized parenchymal volume. Presented here is a case in a 3-month-old male who presented with hypotonia and seizures and was subsequently diagnosed with adenylosuccinate lyase deficiency. Given the rarity of this diagnosis, findings demonstrated in this case may prompt ordering physicians to broaden their approach to genetic testing in the setting of hypomyelination. Comparison is also made to more common hypomyelinating leukodystrophies.