Dominant form of arthrogryposis multiplex congenita with limited mouth opening: A clinical and imaging study

Journal of Orofacial Pain

Volumn 19, Issue 1, 2005, Pages 82-88

  Guimarães, Antonio Sergio ^a,c   Nagahashi Marie, Suely Kazue ^b  

^a FEDERAL UNIVERSITY OF SÃO PAULO   (Brazil)

^b UNIVERSITY OF SÃO PAULO   (Brazil)

^c NONE   (Brazil)

Author keywords

3 Dimensional computed tomography; Arthrogryposis; Coronoid process; Jaw locking; Magnetic resonance imaging; Mouth opening

Indexed keywords

ADOLESCENT; ADULT; AGED; ARTHROGRYPOSIS; ARTICLE; CHILD; CLINICAL ARTICLE; COMPUTER ASSISTED TOMOGRAPHY; FEMALE; HUMAN; HYPERPLASIA; MALE; MANDIBLE CONDYLE; MASTICATION; MOUTH; MUSCLE TISSUE; NUCLEAR MAGNETIC RESONANCE IMAGING; PEDIGREE; ZYGOMA;

ADOLESCENT; ADULT; AGED; AGED, 80 AND OVER; ARTHROGRYPOSIS; CHILD; DIAGNOSIS, DIFFERENTIAL; FEMALE; GENES, DOMINANT; HUMANS; MAGNETIC RESONANCE IMAGING; MALE; MANDIBLE; PEDIGREE; RANGE OF MOTION, ARTICULAR; TEMPOROMANDIBULAR JOINT; TEMPOROMANDIBULAR JOINT DISORDERS; TOMOGRAPHY, X-RAY COMPUTED;

EID: 13544254450     PISSN: 10646655     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (16)

1. Hall JG. An approach to congenital contractures (arthrogryposis). Pediatr Ann 1981;10:15-26.
2. Garfunkel A, Steiner JE. Orofacial manifestations in arthrogryposis: A case report. J Oral Med 1971;26:77-81.
3. Cohen SR, Isaacs H Jr. Otolaryngological manifestations of arthrogryposis multiplex congenita. Ann Otol Rhinol Laryngol 1976;85(4 Pt 1):484-490.
4. Heffez L, Doku HC, O'Donnell JP. Arthrogryposis multiplex complex involving the temporomandibular joint. J Oral Maxillofac Surg 1985;43:539-542.
5. Hageman G, Willemse J. Arthrogryposis multiplex congenita. Review with comment. Neuropediatrics 1983;14: 6-11.
6. Bamshad M, Watkins WS, Zenger RK, et al. A gene for distal arthrogryposis type I maps to the pericentromeric region of chromosome 9. Am J Hum Genet 1994;55: 1153-1158.
7. Krakowiak P, O'Quinn JR, Bohnsack JF, et al. A variant of Freeman-Sheldon syndrome maps to 11 p15.5-pter. Am J Hum Genet 1997;60:426-432.
8. de Andrade CM, Hotta TH, Mazetto MO, de Felicio CM, Bataglion A. Arthrogryposis multiplex congenita in a patient with limited mouth opening: A case report. Cranio 2000;18:66-70.
9. Steinberg B, Nelson VS, Feinberg SE, Calhoun C. Incidence of maxillofacial involvement in arthrogryposis multiplex congenita. J Oral Maxillofac Surg 1996;54: 956-959.
10. Thomas JA, Chiu-Yeh M, Moriconi ES. Maxillofacial implications and surgical treatment of arthrogryposis multiplex congenita. Compend Contin Educ Dent 2001;22: 588-592.
11. Hodgson P, Weinberg S, Consky C. Arthrogryposis multiplex congenita of the temporomandibular joint. Oral Surg Oral Med Oral Pathol 1988;65:289-291.
12. Tasaki MM, Westesson PL. Temporomandibular joint: diagnostic accuracy with sagittal and coronal MR imaging. Radiology 1993;186:723-729.
13. Smith EM, Bender LF, Stover CN. Lower motor neuron deficit in arthrogryposis. An EMG study. Arch Neurol 1963;8:97-100.
14. Staheli LT, Hall JG, Jaffe KM, Paholke DO. Arthrogryposis: A text atlas. Cambridge, UK: Cambridge University Press, 1998.
15. Robertson RD, Spence MA, Sparkes RS, Neiswanger K, Field LL. Linkage analysis with the trismus-pseudocamptodactyly syndrome. Am J Med Genet 1982;12:115-120.
16. Tsukahara M, Shinozaki F, Kajii T. Trismus-pseudocamptodactyly syndrome in a Japanese family. Clin Genet 1985;28:247-250.