| Literature DB >> 28879307 |
Seong In Chi1, Hyun Jeong Kim1, Kwang-Suk Seo1, Jong Ho Lee2, Juhea Chang3.
Abstract
Spinal muscular atrophy (SMA) is an autosomal recessive, severe neuromuscular disorder in which degeneration of alpha motor neurons in the spine progressively weakens and ultimately paralyzes the proximal muscles. It occurs in one per 6,000-10,000 infants, and is a genetic disorder with the second-highest mortality rate worldwide. An 18-year-old male patient with SMA was referred for general anesthesia for difficulty in performing dental treatment due to limited mouth opening caused by temporomandibular joint (TMJ) pain. However, the patient had a high risk of general anesthesia complications, so TMJ pain during mouth opening was reduced through local anesthesia of the TMJ. Fortunately, the anesthesia was successful in reducing pain during mouth opening, enabling the patient to receive dental treatment with an adequate mouth opening.Entities:
Keywords: Dental care for disabled; Spinal muscular atrophy; Temporomandibular joint disorder
Year: 2016 PMID: 28879307 PMCID: PMC5564083 DOI: 10.17245/jdapm.2016.16.2.137
Source DB: PubMed Journal: J Dent Anesth Pain Med ISSN: 2383-9309
Fig. 1One milliliter of 0.5% levobupivacaine each was injected into the right and left TMJ.