Neurosurgical management of a large meningocele in Jarcho-Levin syndrome: clinical and radiological pearls
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منابع مشابه
Neurosurgical management of a large meningocele in Jarcho-Levin syndrome: clinical and radiological pearls.
To cite: Martinez Santos JL, Dmytriw AA, Fermin S. BMJ Case Rep Published online: [please include Day Month Year] doi:10.1136/bcr-2015210240 DESCRIPTION A 4-month-old Dominican girl was born prematurely with numerous malformations (figures 1–4) including facial asymmetry, low-implanted left ear, short neck, short trunk, barrel chest, a left preaxillary thoracic depression, thoracolumbar scolios...
متن کاملJarcho-Levin syndrome.
literature(2,3). Recently, this syndrome has been divided into two major subtypes: spondylothoracic dysostosis and spondylocostal dysostosis(3,4). We describe two cases of the JarchoLevin syndrome, one of each subtype (spondylothoracic dysostosis and spondylocostal dysostosis). The cases illustrate the typical findings of the syndrome and highlight the differences between the two subtypes of th...
متن کاملA child with Jarcho-levin syndrome
In 1938, Jarcho and Levin1 first described a syndrome of congenital abnormalities affecting the spine and the thorax. The syndrome described a spectrum of radiological and skeletal anomalies including abnormal vertebral segmentation or formation defects, rib deformities and short trunk dwarfism. In 1978, Solomon et al2 subdivided patients with the above features into 2 distinct phenotypes: spon...
متن کاملPulmonary hypoplasia in Jarcho-Levin syndrome.
Jarcho-Levin syndrome, also known as spondylothoracic dysplasia and characterized by short trunk dwarfism, "crab-like" rib cage, with ribs and vertebral defects; it is not uncommon in Puerto Ricans. Many patients die in early infancy due to respiratory compromise associated to lung restriction and the reported cases emphasize mostly the skeletal malformations associated to the syndrome. We repo...
متن کاملJarcho Levin Syndrome Associated With Aortic Coarctation
Jarcho-Levin syndrome (JLS) is a rare congenital disorder characterized by the presence of vertebral and rib malformations at birth, first described in 1938 by Jarcho and Levin [1,2]. The majority of reported cases have originated in Puerto Rico, it seems that this syndrome is more common in patients with Spanish ancestors. Its frequency in Spain is 0.2 per 100000 newborns with a female predomi...
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ژورنال
عنوان ژورنال: BMJ Case Reports
سال: 2015
ISSN: 1757-790X
DOI: 10.1136/bcr-2015-210240