Literature DB >> 28214971

Complete occipitalization of the atlas with bilateral external auditory canal atresia.

Janez Dolenšek1, Erika Cvetko1, Žiga Snoj2, Marija Meznaric3.   

Abstract

Fusion of the atlas with the occipital bone is a rare congenital dysplasia known as occipitalization of the atlas, occipitocervical synostosis, assimilation of the atlas, or atlanto-occipital fusion. It is a component of the paraxial mesodermal maldevelopment and commonly associated with other dysplasias of the craniovertebral junction. External auditory canal atresia or external aural atresia is a rare congenital absence of the external auditory canal. It occurs as the consequence of the maldevelopment of the first pharyngeal cleft due to defects of cranial neural crest cells migration and/or differentiation. It is commonly associated with the dysplasias of the structures derived from the first and second pharyngeal arches including microtia. We present the coexistence of the occipitalization of the atlas and congenital aural atresia, an uncommon combination of the paraxial mesodermal maldevelopment, and defects of cranial neural crest cells. The association is most probably syndromic as minimal diagnostic criteria for the oculoariculovertebral spectrum are fulfilled. From the clinical point of view, it is important to be aware that patients with microtia must obtain also appropriate diagnostic imaging studies of the craniovetebral junction due to eventual concomitant occipitalization of the atlas and frequently associated C1-C2 instability.

Entities:  

Keywords:  Craniovertebral junction; External auditory canal atresia; Malformation; Microtia; Occipitalizaton of atlas; Oculoauriculovertebral spectrum

Mesh:

Year:  2017        PMID: 28214971     DOI: 10.1007/s00276-017-1826-y

Source DB:  PubMed          Journal:  Surg Radiol Anat        ISSN: 0930-1038            Impact factor:   1.246


  20 in total

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Review 2.  A case of occipitalization in the human skull.

Authors:  J Skrzat; I Mróz; J K Jaworek; J Walocha
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3.  Craniocervical developmental anatomy and its implications.

Authors:  Arnold H Menezes
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4.  Abnormalities of the spine in Goldenhar's syndrome.

Authors:  J N Gibson; D O Sillence; T K Taylor
Journal:  J Pediatr Orthop       Date:  1996 May-Jun       Impact factor: 2.324

5.  A morphometric study of the atlas occipitalization and coexisted congenital anomalies of the vertebrae and posterior cranial fossa with neurological importance.

Authors:  Konstantinos Natsis; Christos Lyrtzis; Trifon Totlis; Nikolaos Anastasopoulos; Maria Piagkou
Journal:  Surg Radiol Anat       Date:  2016-05-18       Impact factor: 1.246

6.  Osseous anomalies of the craniovertebral junction.

Authors:  R N Hensinger
Journal:  Spine (Phila Pa 1976)       Date:  1986-05       Impact factor: 3.468

7.  Spinal anomalies in Goldenhar syndrome.

Authors:  Peter J Anderson; David J David
Journal:  Cleft Palate Craniofac J       Date:  2005-09

Review 8.  Craniofacial malformations: intrinsic vs extrinsic neural crest cell defects in Treacher Collins and 22q11 deletion syndromes.

Authors:  M B Walker; P A Trainor
Journal:  Clin Genet       Date:  2006-06       Impact factor: 4.438

9.  Oculo-auriculo-vertebral spectrum: clinical and molecular analysis of 51 patients.

Authors:  Ana Beleza-Meireles; Rachel Hart; Jill Clayton-Smith; Renata Oliveira; Cláudia Falcão Reis; Margarida Venâncio; Fabiana Ramos; Joaquim Sá; Lina Ramos; Elizabete Cunha; Luís Miguel Pires; Isabel Marques Carreira; Rachel Scholey; Ronnie Wright; Jill E Urquhart; Tracy A Briggs; Bronwyn Kerr; Helen Kingston; Kay Metcalfe; Dian Donnai; William G Newman; Jorge Manuel Saraiva; May Tassabehji
Journal:  Eur J Med Genet       Date:  2015-07-20       Impact factor: 2.708

Review 10.  Embryology and bony malformations of the craniovertebral junction.

Authors:  Dachling Pang; Dominic N P Thompson
Journal:  Childs Nerv Syst       Date:  2010-12-31       Impact factor: 1.475

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