Article

Mowat-Wilson Syndrome: Growth Charts

2020-05-19

Abstract excerpt

<title>Abstract</title> <p><bold>Background</bold>: Mowat–Wilson syndrome (MWS; OMIM #235730) is a genetic condition caused by heterozygous mutations or deletions of the <italic>ZEB2</italic> gene. It is characterized by moderate-severe intellectual disability, epilepsy, Hirschsprung disease and multiple organ malformations of which congenital heart defects and urogenital anomalies are the most frequent ones. To...

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Literature Corpus work: 2106a442-dd24-55d6-9db1-51fcc562654c
DOI: 10.21203/rs.3.rs-17457/v2

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