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Published in 2019 at "Clinical Endocrinology"
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…
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Keywords:
new presentation;
hypoglycaemia new;
hypoglycaemia;
deletion ... See more keywords
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Published in 2018 at "Indian Journal of Ophthalmology"
DOI: 10.4103/ijo.ijo_1115_17
Abstract: Purpose: Variant myopia (VM) presents as a discrepancy of >1 diopter (D) between subjective and objective refraction, without the presence of any accommodative dysfunction. The purpose of this study is to create a clinical profile…
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Keywords:
presentation;
etiology;
new presentation;
myopia new ... See more keywords