Literature DB >> 14577812

Cleft palate repair in spondyloepiphyseal dysplasia congenita: minimizing the risk of cervical cord compression.

Christopher E Tofield1, Craig A Mackinnon.   

Abstract

OBJECTIVE: Spondyloepiphyseal dysplasia congenita (SEDC) is a rare, inheritable condition that can include dwarfism, cleft palate, and C(1-2) instability. When repairing a cleft palate in a patient with SEDC, there is a significant risk of cord compression at the C(1-2) level because of neck hyperextension required for the operation. This reports presents a patient with SEDC who underwent surgery for a cleft palate, using a Ferno vacuum splint to immobilize the spine. INTERVENTION: The patient underwent general anesthesia. Good access was gained to the palate, and it was repaired without any complications. Particular attention was paid to maintaining the neck in a neutral position.
CONCLUSIONS: The described technique provides the patient with the safest possible situation during anesthesia for cleft palate repair.

Entities:  

Mesh:

Year:  2003        PMID: 14577812     DOI: 10.1597/02-159

Source DB:  PubMed          Journal:  Cleft Palate Craniofac J        ISSN: 1055-6656


  2 in total

1.  A novel mutation in COL2A1 leading to spondyloepiphyseal dysplasia congenita in a three-generation family.

Authors:  Leilei Xu; Xusheng Qiu; Zezhang Zhu; Long Yi; Yong Qiu
Journal:  Eur Spine J       Date:  2014-04-16       Impact factor: 3.134

2.  Identification of a novel mutation of the COL2A1 gene in a Chinese family with spondyloepiphyseal dysplasia congenita.

Authors:  Hongzhuo Li; Liang Ma; Baozhu Wang; Yun Cui; Tao Xiao
Journal:  Eur Spine J       Date:  2015-05-13       Impact factor: 3.134

  2 in total

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