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

• Үндсэн зохиолчид: Panicos Shangaris (Зохиогч), Alison Ho (Зохиогч), Andreas Marnerides (Зохиогч), Simi George (Зохиогч), Mudher AlAdnani (Зохиогч), Shu Yau (Зохиогч), Mattias Jansson (Зохиогч), Jacqueline Hoyle (Зохиогч), Joo Wook Ahn (Зохиогч), Sian Ellard (Зохиогч), Melita Irving (Зохиогч), Diana Wellesley (Зохиогч), Dharmintra Pasupathy (Зохиогч), Muriel Holder-Espinasse (Зохиогч)
• Формат: Ном
• Хэвлэсэн: BMC, 2021-02-01T00:00:00Z.
• Нөхцлүүд: article
• Онлайн хандалт: Connect to this object online.

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...