Jarcho-Levin syndrome.

نویسندگان

  • M Suri
  • Madhulika
  • H Pemde
  • A K Gupta
  • I C Verma
چکیده

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 this syndrome.

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گزارش یک مورد Jarcho-Levin syndrom در یک شیرخوار دو ماهه و ترمیم فتق مغبنی با مش

Jarcho-Levin syndrome a very rare anomaly is described for a variety of clinical phenotypes consisting of short-trunk dwarfism associated with rib and vertebral anomalies. The patient is two months old infant with spondylocostal dysostosis and bilateral direct recurrent inguinal hernia. He was successfully operated by a new method and after 36 months follow up he did not have any problem.

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Jarcho 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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Airway abnormalities in Jarcho-Levin syndrome: a report of two cases.

Two infants with the Jarcho-Levin syndrome of vertebral anomalies underwent flexible fibre optic bronchoscopy. Central airway abnormalities not amenable to surgical correction were found in both patients. These abnormalities may contribute significantly to the respiratory failure seen in affected infants, and should be considered when evaluating continuing medical support.

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عنوان ژورنال:
  • Indian pediatrics

دوره 31 6  شماره 

صفحات  -

تاریخ انتشار 1994