Hyperinsulinaemic hypoglycaemia: A new presentation of 16p11.2 deletion syndrome
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DOI: 10.1111/cen.13951
Abstract: 16p11.2 microdeletion syndrome is a recognisable chromosomal anomaly caused by microdeletions in the 16p11.2 locus. It is characterized by developmental delay intellectual disability and social impairments or susceptibility to autism spectrum disorder. It also involves… read more here.
Keywords: new presentation; hypoglycaemia new; hypoglycaemia; deletion ... See more keywords