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Published in 2022 at "Ophthalmic genetics"
DOI: 10.1080/13816810.2022.2121968
Abstract: BACKGROUND Verheij syndrome (VRJS) is a rare microdeletion syndrome of chromosome 8q24.3 that is characterized by severe growth retardation, microcephaly, vertebral anomalies, joint laxity/dislocation, psychomotor retardation, cardiac and renal defects, and dysmorphic facial features. Pathogenic…
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Keywords:
cord syndrome;
report;
patient verheij;
tethered cord ... See more keywords