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For this reason, every child with ASD and seizures should have a comprehensive medical evaluation for known medical disorders that includes the following: A genetic workup, consisting of a chromosomal microarray, Fragile X, and Rett syndrome testing If these return normal, further testing may include an epilepsy genetic panel or whole exome genetic sequencing
DPP4 , DPP4 GLP-1 homeostatic model-insulin resistance, IL-6, high sensitivity C reactive protein [36]
Although the diagnosis and preventative strategy may be rather straightforward, much is unclear about the pathophysiology and heterogeneity of this inherited genetic condition that underlies the severity of neonatal hyperbilirubinemia
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