| Literature DB >> 21934288 |
H Le Borgne1, H J Philippe, C Le Vaillant.
Abstract
Cloacal anomaly is a rare malformation with an incidence of 1 in 50,000 births. The definitive prenatal diagnosis of cloacal dysgenesis sequence is difficult. The use of three-dimensional (3-D) ultrasonography helps to describe the perineum and change diagnosis. In our case report, a large median genital structure was visualized, which was initially considered a penis-like structure, but the 3-D technique showed an enlarged bud. The urethral meatus was at the tip of this smooth structure. The lack of anal structure was clearly demonstrated.Entities:
Mesh:
Year: 2011 PMID: 21934288 DOI: 10.1159/000331447
Source DB: PubMed Journal: Fetal Diagn Ther ISSN: 1015-3837 Impact factor: 2.587