Literature DB >> 15692209

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

María del Río Holgado1, Josep M Martínez, Olga Gómez, Gemma Casals, Nuria Bargalló, Albert Fortuny, Bienvenido Puerto.   

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. Copyright (c) 2005 S. Karger AG, Basel.

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Year:  2005        PMID: 15692209     DOI: 10.1159/000082438

Source DB:  PubMed          Journal:  Fetal Diagn Ther        ISSN: 1015-3837            Impact factor:   2.587


  3 in total

1.  Posterior vertebral column resection for VATER/VACTERL associated spinal deformity: a case report.

Authors:  Matthew E Cunningham; Gina Charles; Oheneba Boachie-Adje
Journal:  HSS J       Date:  2007-02

2.  Fetal diagnosis of spondylocostal dysplasia: Limits of conventional fetal ultrasound & MRI in diagnosing anomalies.

Authors:  Teresa Chapman; Stephen Done; Michael Goldberg
Journal:  Radiol Case Rep       Date:  2015-11-06

3.  A rare case of fetal spondylocostal dysostosis - prenatal diagnosis and perinatal care in a patient with multiple large leiomyomas.

Authors:  M Cirstoiu; O Munteanu; O Bodean; C Cirstoiu
Journal:  J Med Life       Date:  2013-03-25
  3 in total

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