Literature DB >> 4019764

Combined occipitoatlantoaxial hypermobility with anterior and posterior arch defects of the atlas in Pierre-Robin syndrome.

J G Gamble, L A Rinsky.   

Abstract

Combined occipitoatlantoaxial instability of the cervical spine occurred in a 8-year-3-month old boy with Pierre-Robin syndrome. He also had failure of ossification of both the anterior and posterior arches of the atlas. An in situ fusion from the occiput to C2 restored cervical spine stability. This case is discussed in relation to other hypermobility and instability syndromes of the cervical spine.

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Year:  1985        PMID: 4019764     DOI: 10.1097/01241398-198507000-00018

Source DB:  PubMed          Journal:  J Pediatr Orthop        ISSN: 0271-6798            Impact factor:   2.324


  7 in total

1.  Cervico-thoracic kyphosis in a girl with Pierre Robin sequence.

Authors:  Ali Al Kaissi; Rudolf Ganger; Klaus Klaushofer; Franz Grill
Journal:  Ger Med Sci       Date:  2011-03-14

2.  Pierre-Robin syndrome associated with Chiari type I malformation.

Authors:  Jangbo Lee; Kazutoshi Hida; Toshitaka Seki; Jun Kitamura; Yosinobu Iwasaki
Journal:  Childs Nerv Syst       Date:  2003-05-14       Impact factor: 1.475

3.  The incidence and clinical implications of congenital defects of atlantal arch.

Authors:  Jong Kyu Kwon; Myoung Soo Kim; Ghi Jai Lee
Journal:  J Korean Neurosurg Soc       Date:  2009-12-31

4.  C1-2 vertebral anomalies in 22q11.2 microdeletion syndrome.

Authors:  Osnat Konen; Derek Armstrong; Howard Clarke; Nancy Padfield; Rosanna Weksberg; Susan Blaser
Journal:  Pediatr Radiol       Date:  2008-05-31

5.  Krapina atlases suggest a high prevalence of anatomical variations in the first cervical vertebra of Neanderthals.

Authors:  Carlos A Palancar; Daniel García-Martínez; Davorka Radovčić; Susanna Llidó; Federico Mata-Escolano; Markus Bastir; Juan Alberto Sanchis-Gimeno
Journal:  J Anat       Date:  2020-05-21       Impact factor: 2.921

6.  A Novel 12q13.2-q13.3 Microdeletion Syndrome With Combined Features of Diamond Blackfan Anemia, Pierre Robin Sequence and Klippel Feil Deformity.

Authors:  Domenico Roberti; Renata Conforti; Teresa Giugliano; Barbara Brogna; Immacolata Tartaglione; Maddalena Casale; Giulio Piluso; Silverio Perrotta
Journal:  Front Genet       Date:  2018-11-19       Impact factor: 4.599

Review 7.  Clinical and genetic characterization of patients with Pierre Robin sequence and spinal disease: review of the literature and novel terminal 10q deletion.

Authors:  Anudeep Yekula; Connor Grant; Mihir Gupta; David R Santiago-Dieppa; Pate J Duddleston; David Gonda; Michael Levy
Journal:  Childs Nerv Syst       Date:  2020-05-12       Impact factor: 1.475

  7 in total

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