Literature DB >> 32537787

Fetal hydrometrocolpos with pre-axial mirror polydactyly as a new variant of McKusick-Kaufman syndrome.

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.
© 2020 Wiley Periodicals, Inc.

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


  1 in total

1.  A case of McKusick-Kaufman syndrome with perinatal diagnosis: Case report and literature review.

Authors:  Irfan Ullah; Shahzad Rauf; Sajjad Ali; Kiran Shafiq Khan; Tayyaba Zahid; Jahanzeb Malik; Rifayat Ullah Afridi; Muhammad Sohaib Asghar
Journal:  Ann Med Surg (Lond)       Date:  2022-06-06
  1 in total

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