| Literature DB >> 33210306 |
Dongmei Yu1, Lingyu Sun1, Taotao Chen1.
Abstract
We describe a case of prenatal diagnosed Klippel-Trenaunay-Weber syndrome, which mainly manifested as hypertrophy of the left thigh, and was associated with umbilical cord hemangioma and loss of heterozygosity (LOH) for 1q21.2 q44. This case report describes the second reported case associated with umbilical cord hemangioma and the first reported case with LOH for 1q21.2 q44.Entities:
Keywords: Klippel-Trenaunay-Weber syndrome; chromosome abnormality; prenatal diagnosis; ultrasound
Mesh：
Year: 2020 PMID： 33210306 DOI： 10.1002/jcu.22896
Source DB: PubMed Journal: J Clin Ultrasound ISSN： 0091-2751 Impact factor: 0.910