noun
Meaning 1
A rare genetic disorder caused by a deletion of a segment of chromosome 17 containing six genes, commonly resulting in low birthweight and muscle tone at birth, poor feeding in infancy, and oromotor dyspraxia together with moderate developmental delays and learning disabilities.
Definition source: English Wiktionary via Wiktextract
Usage: uncountable
No example sentence was provided for this meaning.
Meaning relationships
Synonyms: 17q21.31 microdeletion syndrome, KdVS
Antonyms: none provided