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Prenatal ultrasound diagnosis of Klippel‐Trenaunay‐Weber syndrome associated with umbilical cord hemangioma
Author(s) -
Yu Dongmei,
Sun Lingyu,
Chen Taotao
Publication year - 2020
Publication title -
journal of clinical ultrasound
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.272
H-Index - 61
eISSN - 1097-0096
pISSN - 0091-2751
DOI - 10.1002/jcu.22896
Subject(s) - medicine , umbilical cord , hemangioma , ultrasonogram , prenatal diagnosis , ultrasound , cord , thigh , single umbilical artery , fetus , ultrasonography , anatomy , pregnancy , pathology , surgery , radiology , genetics , biology
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.