Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
8782057 | Journal of Pediatric and Adolescent Gynecology | 2018 | 16 Pages |
Abstract
Müllerian aplasia/hypoplasia might represent a rare feature in CES and should be considered in the investigation of young girls with this syndrome. An increasing number of cases with 22q11 chromosome abnormalities and Müllerian agenesis further highlights the possibility of a gene within the 22q11 region that might mediate normal Müllerian development in girls.
Keywords
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Authors
Abdulmajeed MBBS, FRCPC, John MD, PhD, FRCPC, Kate MSc, John BSc, Elizabeth PhD, MSc, FCCMG,