Mowat–Wilson syndrome – case study

Mowat–Wilson syndrome is a rare genetic condition characterised by a number of congenital anomalies, including facial dysmorphia, heart and kidney anomalies, Hirschsprung’s disease, intellectual disability and abnormalities of reproductive organs. In the paper, we present a case of a girl who was...

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書誌詳細

出版年:	Pediatria i Medycyna Rodzinna
主要な著者:	Kamil Faltin, Marta Kostrzewa, Małgorzata Stańczyk, Marcin Tkaczyk
フォーマット:	論文
言語:	英語
出版事項:	Medical Communications Sp. z o.o. 2016-06-01
主題:	Mowat–Wilson syndrome Hirschsprung’s disease mental retardation congenital defects
オンライン･アクセス:	http://www.pimr.pl/index.php/issues/2016-vol-12-no-2/mowat-wilson-syndrome-case-study?aid=958