Premature ovarian insufficiency as a variable feature of blepharophimosis, ptosis, and epicanthus inversus syndrome associated with c.223C > T p.(Leu75Phe) FOXL2 mutation: a case report
Abstract Background FOXL2 gene mutations cause blepharophimosis-ptosis-epicanthus inversus syndrome (BPES) and may be associated with premature ovarian insufficiency (POI). Two types of BPES were described in the literature. BPES type 2 is a simple association of inherited developmental defects of t...
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Main Authors: | Barbara Grzechocińska (Author), Damian Warzecha (Author), Maria Wypchło (Author), Rafal Ploski (Author), Mirosław Wielgoś (Author) |
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Format: | Book |
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BMC,
2019-07-01T00:00:00Z.
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Online Access: | Connect to this object online. |
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