Skip to main content
Top
Published in: Pediatric Rheumatology 1/2007

Open Access 01-12-2007 | Case Report

Ischiopubic and odontoid synchondrosis in a boy with progressive pseudorheumatoid chondrodysplasia

Authors: Ali Al Kaissi, Farid Ben Chehida, Maher Ben Ghachem, Franz Grill, Klaus Klaushofer

Published in: Pediatric Rheumatology | Issue 1/2007

Login to get access

Abstract

Purpose

To present the case of a 14-year-old boy with clinical and radiographic features of pseudorheumatoid chondrodyspalsia with additional, potentially serious, cervical malformations.

Methods

Detailed clinical and radiological examinations were undertaken with emphasis on the usefulness of 3D-CT scanning.

Results

There was synchondrosis between the odontoid and the body of the axis and the cephalad part of the odontoid was detached. Bilateral ischiopubic ossification defects and ischiopubic and odontoid synchondroses were additional abnormalities. 3D-CT scan showed an orthotopic type of os odontoideum associated with an occult axial fracture.

Conclusion

Children who are younger than seven years of age are predisposed to develop odontoid fracture. The latter occur because of the presence of physiological odontoid synchondrosis, but fractures can result from trivial injuries as well as from high-energy trauma. The persistence of an infantile odontoid, with a large pre-adulthood head in children with skeletal dysplasias, is a major risk factor for sudden death or significant morbidity. Comprehensive orthopaedic management must follow early identification of these malformations.
Appendix
Available only for authorised users
Literature
1.
go back to reference Spranger JW, Brill PW, Poznanski A: Reprint [2002]. Bone dysplasias. An atlas of genetic disorders of skeletal development. Ed:Oxford. 186-189. Spranger JW, Brill PW, Poznanski A: Reprint [2002]. Bone dysplasias. An atlas of genetic disorders of skeletal development. Ed:Oxford. 186-189.
2.
go back to reference Spranger J, Albert C, Schilling F: A progressive connective tissue disease with features of juvenile rheumatoid arthritis and osteochondrodysplasia. Eur J Pediatr. 1980, 133: 186- Spranger J, Albert C, Schilling F: A progressive connective tissue disease with features of juvenile rheumatoid arthritis and osteochondrodysplasia. Eur J Pediatr. 1980, 133: 186-
3.
go back to reference Spranger J, Albert C, Schilling F, Bartsocas C, Stoss H: Progressive pseudorheumatoid arthritis of childhood (PPAC). A hereditary disorder simulating rheumatoid arthritis. Eur J Pediatr. 1983, 140: 34-40. 10.1007/BF00661902.CrossRefPubMed Spranger J, Albert C, Schilling F, Bartsocas C, Stoss H: Progressive pseudorheumatoid arthritis of childhood (PPAC). A hereditary disorder simulating rheumatoid arthritis. Eur J Pediatr. 1983, 140: 34-40. 10.1007/BF00661902.CrossRefPubMed
4.
go back to reference Poznanski AK: Comments on the ischio-pubic-patellar syndrome. Pediatr Radiol. 1997, 27: 428-429. 10.1007/s002470050161.CrossRefPubMed Poznanski AK: Comments on the ischio-pubic-patellar syndrome. Pediatr Radiol. 1997, 27: 428-429. 10.1007/s002470050161.CrossRefPubMed
5.
go back to reference Odelberg A: Some cases of destruction in the ischium of doubtful etiology. Acta Chir Scand. 1924, 56: 273- Odelberg A: Some cases of destruction in the ischium of doubtful etiology. Acta Chir Scand. 1924, 56: 273-
7.
go back to reference El-Shanti H, Murray JC, Semina EV, Beutow KH, Scherpbier T, Al-Alami J: Assignment of gene responsible for progressive pseudorheumatoid dysplasia to chromosome 6 and examination of COL1OA1 as a candidate gene. Eur J Hum Genet. 1998, 6: 251-256. 10.1038/sj.ejhg.5200187.CrossRefPubMed El-Shanti H, Murray JC, Semina EV, Beutow KH, Scherpbier T, Al-Alami J: Assignment of gene responsible for progressive pseudorheumatoid dysplasia to chromosome 6 and examination of COL1OA1 as a candidate gene. Eur J Hum Genet. 1998, 6: 251-256. 10.1038/sj.ejhg.5200187.CrossRefPubMed
8.
go back to reference Fischer J, Urtizberea JA, Pavek S, Vandiedonck C, Bruls T, Saker S, Alkatip Y, Prud'homme JF, Weissenbach J: Genetic linkage of progressive pseudorheumatoid dysplasia to a 3-cM interval of chromosome 6q22. Hum Genet. 1998, 103: 60-64. 10.1007/s004390050784.CrossRefPubMed Fischer J, Urtizberea JA, Pavek S, Vandiedonck C, Bruls T, Saker S, Alkatip Y, Prud'homme JF, Weissenbach J: Genetic linkage of progressive pseudorheumatoid dysplasia to a 3-cM interval of chromosome 6q22. Hum Genet. 1998, 103: 60-64. 10.1007/s004390050784.CrossRefPubMed
9.
go back to reference Hurvitz JR, Suwairi WM, Van Hul W, El-Shanti H, Superti-Furga A, Roudier J, Holderbaum D, Pauli RM, Herd JK, Van Hul EV, Rezai-Delui H, Legius E, Le Merrer M, Al-Alami J, Bahabri SA, Warman ML: Mutations in the CCN gene family member WISP3 cause progressive pseudorheumatoid dysplasia. Nature Genetics. 1999, 23: 94-97. 10.1038/12699.CrossRefPubMed Hurvitz JR, Suwairi WM, Van Hul W, El-Shanti H, Superti-Furga A, Roudier J, Holderbaum D, Pauli RM, Herd JK, Van Hul EV, Rezai-Delui H, Legius E, Le Merrer M, Al-Alami J, Bahabri SA, Warman ML: Mutations in the CCN gene family member WISP3 cause progressive pseudorheumatoid dysplasia. Nature Genetics. 1999, 23: 94-97. 10.1038/12699.CrossRefPubMed
10.
go back to reference Wynne-Davies R, Hall C, Ansell BM: Spondylo-epiphyseal dysplasia tarda with progressive arthropathy. A 'new' disorder of autosomal recessive inheritance. J Bone Joint Surg Br. 1982, 64 (4): 442-445.PubMed Wynne-Davies R, Hall C, Ansell BM: Spondylo-epiphyseal dysplasia tarda with progressive arthropathy. A 'new' disorder of autosomal recessive inheritance. J Bone Joint Surg Br. 1982, 64 (4): 442-445.PubMed
11.
go back to reference Oestreich AE: Mega os trigonum in progressive pseudorheumatoid dysplasia. Pediatr Radiol. 2002, 32: 46-8. 10.1007/s00247-001-0576-4.CrossRefPubMed Oestreich AE: Mega os trigonum in progressive pseudorheumatoid dysplasia. Pediatr Radiol. 2002, 32: 46-8. 10.1007/s00247-001-0576-4.CrossRefPubMed
12.
go back to reference Marik I, Marikova O, Zemkova D, Kuklik M, Kozlowski K: Dominantly inherited progressive pseudorheumatoid dysplasia with hypoplastic toes. Skeletal Radiol. 2004, 33: 157-164. 10.1007/s00256-003-0708-z.CrossRefPubMed Marik I, Marikova O, Zemkova D, Kuklik M, Kozlowski K: Dominantly inherited progressive pseudorheumatoid dysplasia with hypoplastic toes. Skeletal Radiol. 2004, 33: 157-164. 10.1007/s00256-003-0708-z.CrossRefPubMed
13.
go back to reference Wollin DG: The os odontoideum: separate odontoid process. J Bone Joint Surg Am. 1963, 45: 1459-1471.PubMed Wollin DG: The os odontoideum: separate odontoid process. J Bone Joint Surg Am. 1963, 45: 1459-1471.PubMed
14.
go back to reference Lachman SR: The cervical spine in the skeletal dysplasias and associated disorders. Pediatr Radiol. 1997, 27: 402-408. 10.1007/s002470050156.CrossRefPubMed Lachman SR: The cervical spine in the skeletal dysplasias and associated disorders. Pediatr Radiol. 1997, 27: 402-408. 10.1007/s002470050156.CrossRefPubMed
15.
go back to reference Fielding JW, Hensinger RN, Hawkins RJ: Os odontoideum. J Bone Joint Surg Am. 1980, 62 (3): 376-383.PubMed Fielding JW, Hensinger RN, Hawkins RJ: Os odontoideum. J Bone Joint Surg Am. 1980, 62 (3): 376-383.PubMed
16.
go back to reference Currarino G: Segmentation defect in the midodontoid process and its possible relationship to the congenital type of os odontoideum. Pediatr Radiol. 2002, 32: 34-40. 10.1007/s00247-001-0579-1.CrossRefPubMed Currarino G: Segmentation defect in the midodontoid process and its possible relationship to the congenital type of os odontoideum. Pediatr Radiol. 2002, 32: 34-40. 10.1007/s00247-001-0579-1.CrossRefPubMed
17.
go back to reference Dubousset J, Haddad F, Zeller R, Queneau P: La dysplasie ischio-vertebrale (un dangereux syndrome pour la moelle epiniere): ischio vertebral dysplasia. Rev Chir Orthop. 1994, 180: 610-619. Dubousset J, Haddad F, Zeller R, Queneau P: La dysplasie ischio-vertebrale (un dangereux syndrome pour la moelle epiniere): ischio vertebral dysplasia. Rev Chir Orthop. 1994, 180: 610-619.
18.
go back to reference Cohen PA, Kalifa G, Donoghue V, Haddad F, Dubousset J: Ischio-vertebral dysplasia: a distinct entity. Pediatr Radiol. 1999, 29: 131-134. 10.1007/s002470050556.CrossRefPubMed Cohen PA, Kalifa G, Donoghue V, Haddad F, Dubousset J: Ischio-vertebral dysplasia: a distinct entity. Pediatr Radiol. 1999, 29: 131-134. 10.1007/s002470050556.CrossRefPubMed
19.
go back to reference Al Kaissi A, Ben Chehida F, Latos-Bielenska A, Gharbi A, Ben Ghachem M, Hendaoui L, Kozlowski K: A novel form of ischio-vertebral syndrome. Skeletal Radiol. 2007, 36 (1): 77-81. 10.1007/s00256-005-0073-1.CrossRef Al Kaissi A, Ben Chehida F, Latos-Bielenska A, Gharbi A, Ben Ghachem M, Hendaoui L, Kozlowski K: A novel form of ischio-vertebral syndrome. Skeletal Radiol. 2007, 36 (1): 77-81. 10.1007/s00256-005-0073-1.CrossRef
20.
go back to reference Michaels L, Path MC, Prevost MJ: Pathological changes in a case of os odontoideum(separate odontoid process). J Bone Surg Am. 1969, 51: 965-972.PubMed Michaels L, Path MC, Prevost MJ: Pathological changes in a case of os odontoideum(separate odontoid process). J Bone Surg Am. 1969, 51: 965-972.PubMed
21.
go back to reference Julh M, Seerup KK: Os odontoideum: a cause of atlanto-axial instability. Acta Orthop Scand. 1983, 54: 113-118.CrossRef Julh M, Seerup KK: Os odontoideum: a cause of atlanto-axial instability. Acta Orthop Scand. 1983, 54: 113-118.CrossRef
22.
go back to reference Sherk HH, Dawoud S: Congenital os odontoideum with Klippel-Feil anomaly and fatal atlanto-axial instability. Report of a case. Spine. 1981, 6 (1): 42-45. 10.1097/00007632-198101000-00007.CrossRefPubMed Sherk HH, Dawoud S: Congenital os odontoideum with Klippel-Feil anomaly and fatal atlanto-axial instability. Report of a case. Spine. 1981, 6 (1): 42-45. 10.1097/00007632-198101000-00007.CrossRefPubMed
23.
go back to reference Winter RM, Baraitser M: London Dysmorphology database, London Medical Databases, Version 1.0.4 [CD-ROM]. 2005 Winter RM, Baraitser M: London Dysmorphology database, London Medical Databases, Version 1.0.4 [CD-ROM]. 2005
Metadata
Title
Ischiopubic and odontoid synchondrosis in a boy with progressive pseudorheumatoid chondrodysplasia
Authors
Ali Al Kaissi
Farid Ben Chehida
Maher Ben Ghachem
Franz Grill
Klaus Klaushofer
Publication date
01-12-2007
Publisher
BioMed Central
Published in
Pediatric Rheumatology / Issue 1/2007
Electronic ISSN: 1546-0096
DOI
https://doi.org/10.1186/1546-0096-5-19

Other articles of this Issue 1/2007

Pediatric Rheumatology 1/2007 Go to the issue