| Literature DB >> 32537787 |
Kuntharee Traisrisilp1, Sujinun Nunthapiwat1, Suchaya Luewan1, Theera Tongsong1.
Abstract
This report describes a variant of McKusick-Kaufman syndrome presenting with a large fetal abdominal cyst of hydrometrocolpos at 37 weeks of gestation. The diagnosis was based on the ultrasound findings of a large homogeneous hypoechoic cyst (diameter of >10 cm) with incomplete septum, thickened wall, superiorly connecting to the dilated uterus, consistent with hydrometrocolpos. Additionally, pre-axial mirror polydactyly of the left foot was suspected. Postnatal examination/work-up confirmed the prenatal findings. This is the first report of prenatal diagnosis of hydrometrocolpos with complex polydactyly of mirror image pre-axial duplications containing nine toes instead of six-toe postaxial polydactyly.Entities:
Keywords: Bardet-Biedl syndrome; Mckusick-Kaufman syndrome; ambiguous genitalia; hydrometrocolpos; polydactyly; ultrasonography
Mesh:
Year: 2020 PMID: 32537787 DOI: 10.1002/jcu.22882
Source DB: PubMed Journal: J Clin Ultrasound ISSN: 0091-2751 Impact factor: 0.910