Please use this identifier to cite or link to this item: http://hdl.handle.net/10553/43665
Title: Klippel-Feil syndrome and levo-looped transposition of the great arteries
Authors: Martínez Quintana, Efrén 
Rodríguez-González, Fayna
UNESCO Clasification: 320501 Cardiología
Keywords: Heart defect
Issue Date: 2015
Publisher: 1047-9511
Journal: Cardiology in the Young 
Abstract: Klippel-Feil syndrome is a skeletal disorder characterised by low hairline and a short neck due to abnormal fusion of two or more cervical vertebrae. Although congenital heart and lung defects are infrequent, some abnormalities such as cor triatriatum, coarctation of the aorta, total anomalous pulmonary venous connection, or lung agenesis have been reported. The challenge of recognising Klippel-Feil syndrome lies in the fact that there is an association of this syndrome with other significant conditions such as skeletal, genitourinary, neurological, ear, and some cardiac defects. We report a Klippel-Feil syndrome type III 14-year-old patient with a levo-looped transposition of the great arteries. In addition, the patient had agenesis of the left upper-lung lobe.
URI: http://hdl.handle.net/10553/43665
ISSN: 1047-9511
DOI: 10.1017/S1047951114000808
Source: Cardiology in the Young [ISSN 1047-9511], v. 25, p. 591-593
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