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Published in 2017 at "Research in developmental disabilities"
DOI: 10.1016/j.ridd.2017.01.006
Abstract: BACKGROUND Mowat-Wilson Syndrome (MWS) is caused by deletion/mutation of the ZEB2 gene on chromosome 2q22. MWS is characterized by a distinctive facial appearance, severe intellectual disability and other anomalies, e.g. seizures and/or Hirschsprung disease (HSCR).…
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Keywords:
psychological symptoms;
incontinence psychological;
incontinence;
mowat wilson ... See more keywords