Anesthetic Management of Cesarean Section in a Patient with Léri-Weill Dyschondrosteosis – A Case Report
Author:
Affiliation:
1. Michael G. DeGroote School of Medicine, McMaster University, Hamilton, ON, Canada
2. Department of Anesthesiology, McMaster University, Hamilton, ON, Canada
Abstract
Publisher
Medknow
Reference11 articles.
1. A novel class of Pseudoautosomal region 1 deletions downstream of SHOX is associated with Leri-Weill dyschondrosteosis [published correction appears in Am J Hum Genet 2005;77:1131. [Huber, Celine [corrected to Huber, Céline];Del Blanco, Darya Gorbenko [corrected to Gorbenko del Blanco, Darya];Rappold, Gudrun [added];Argente, Jesus [corrected to Argente, Jesús];Cormier-Daire, Valerie [corrected to Cormier-Daire, Valrie]];Benito-Sanz;Am J Hum Genet,2005
2. Dyschondrostéose (Leri-Weill syndrome):Congenital short forearms, Madelung-type wrist deformities, and moderate dwarfism;Berdon;Radiology,1965
3. Mutation and deletion of the pseudoautosomal gene SHOX cause Leri-Weill dyschondrosteosis;Shears;Nat Genet,1998
4. The human Pseudoautosomal region (PAR):Origin, function and future;Helena Mangs;Curr Genomics,2007
5. Clinical and radiological characteristics of 22 children with SHOX anomalies and familial short stature suggestive of Léri-Weill dyschondrosteosis;Salmon-Musial;Horm Res Paediatr,2011
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