A hemizygous mutation in the FOXP3 gene (IPEX syndrome) resulting in recurrent X-linked fetal hydrops: a case report

A hemizygous mutation in the FOXP3 gene (IPEX syndrome) resulting in recurrent X-linked fetal hydrops: a case report

Abstract Background Fetal hydrops is excessive extravasation of fluid into the third space in a fetus, which could be due to a wide differential of underlying pathology. IPEX (immune dysregulation, polyendocrinopathy, enteropathy, X-linked) syndrome primarily affects males. It is a monogenic primary...

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Main Authors: Panicos Shangaris (Author), Alison Ho (Author), Andreas Marnerides (Author), Simi George (Author), Mudher AlAdnani (Author), Shu Yau (Author), Mattias Jansson (Author), Jacqueline Hoyle (Author), Joo Wook Ahn (Author), Sian Ellard (Author), Melita Irving (Author), Diana Wellesley (Author), Dharmintra Pasupathy (Author), Muriel Holder-Espinasse (Author)
Format: Book
Published: BMC, 2021-02-01T00:00:00Z.
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