Symptoms of mild hypoglycemia are easily overlooked especially when there are no complaints from the patients, but it could be a warning sign of an underlying genetic disease. Genetic testing for the entire family is a key step in neonatal hypoglycemia workup.
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Source |
|---|---|
| http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9731303 | PMC |
| http://dx.doi.org/10.1002/ccr3.6636 | DOI Listing |
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