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Ultrasonographic diagnosis of Jarcho-Levin syndrome at 20 weeks' gestation in a fetus without previous family history.

Authors :
del Río Holgado M
Martínez JM
Gómez O
Casals G
Bargalló N
Fortuny A
Puerto B
Source :
Fetal diagnosis and therapy [Fetal Diagn Ther] 2005 Mar-Apr; Vol. 20 (2), pp. 136-40.
Publication Year :
2005

Abstract

Jarcho-Levin syndrome (JLS; spondylothoracic dysplasia) is a congenital disease characterized by multiple vertebral and rib malformations, causing a short trunk dwarfism commonly leading to respiratory insufficiency and death during the first years of life. We describe a case diagnosed during the second trimester routine ultrasound scan for screening of fetal anomalies without a previous family history. The fetus had a severe disorganization of the spine and ribs, skeletal kyphosis, with several hemivertebrae and a small thorax. All of the findings at postmortem examination confirmed the ultrasound features and were consistent with the JLS. To the best of our knowledge there is only one case reported in the literature of a prenatal diagnosis of the syndrome in a family with low risk for the condition.<br /> (Copyright (c) 2005 S. Karger AG, Basel.)

Details

Language :
English
ISSN :
1015-3837
Volume :
20
Issue :
2
Database :
MEDLINE
Journal :
Fetal diagnosis and therapy
Publication Type :
Academic Journal
Accession number :
15692209
Full Text :
https://doi.org/10.1159/000082438