Congenital Trismus From Brainstem Dysgenesis: Case Report and Review of Literature

Author:

Hong Chris J.1,Caulley Lisa12,Kohlert Scott12,Graham Gail E.3,McMillan Hugh J.4,Michaud Jean5,Vaccani Jean-Philippe6

Affiliation:

1. Faculty of Medicine, University of Ottawa, Ottawa, Ontario, Canada;

2. Department of Otolaryngology-Head and Neck Surgery, University of Ottawa, The Ottawa Hospital, Ottawa, Ontario, Canada; and

3. Departments of Genetics,

4. Neurology,

5. Pathology and Laboratory Medicine, and

6. Otolaryngology-Head and Neck Surgery, University of Ottawa, Children’s Hospital of Eastern Ontario, Ottawa, Ontario, Canada

Abstract

Trismus refers to any condition inducing limited mouth opening and may present as a result of acquired or congenital pathology. We present the case of a newborn who presented with severe, congenital trismus due to brainstem dysgenesis. We describe the course of his investigations, and a multidisciplinary approach to the management of his care and follow-up. To our knowledge, this is one of the earliest reported cases of congenital trismus attributable to brainstem dysgenesis. A literature review was conducted to provide an overview of the differential pathogenesis as it presents in congenital cases and discuss the complexity of managing congenital trismus due to brainstem dysgenesis in a neonate and infant.

Publisher

American Academy of Pediatrics (AAP)

Subject

Pediatrics, Perinatology, and Child Health

Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Orofacial motor dysfunction in Moebius syndrome;Developmental Medicine & Child Neurology;2019-11-12

2. Disgenesia troncoencefálica: más allá del síndrome de Moebius;Revista de Neurología;2018

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