Literature DB >> 18369644

Specific entities affecting the craniocervical region: syndromes affecting the craniocervical junction.

Arnold H Menezes1, Timothy W Vogel.   

Abstract

INTRODUCTION: The craniocervical junction is a vital component in understanding the function of the human central nervous system. It is the threshold for major pathways affecting both brain and spinal cord function, and these structures are intricately housed in a network of bone, ligaments, and soft tissues. Abnormal development of any of these components may lead to altered structure, and therefore, altered function in the central nervous system.
MATERIALS AND METHODS: We herein describe a set of genetic syndromes that commonly affect the craniovertebral junction and offer clinical examples from more than 6,000 patients who have been treated for these disorders. DISCUSSION: The syndromes described include Chiari type I malformation, Conradi syndrome, Goldenhar syndrome, Klippel-Feil syndrome, Larsen syndrome, Morquio syndrome, Pierre-Robin syndrome, spondyloepiphyseal dysplasia congenital and Weaver syndrome. The genetic mechanisms responsible for these disorders may offer unique insight into the developmental pathways and patterning in the musculoskeletal and cranial systems and may, ultimately, guide future diagnosis and treatment.

Entities:  

Mesh:

Year:  2008        PMID: 18369644     DOI: 10.1007/s00381-008-0608-6

Source DB:  PubMed          Journal:  Childs Nerv Syst        ISSN: 0256-7040            Impact factor:   1.475


  88 in total

1.  Dominant transmission of a previously unidentified 13/17 translocation in a five-generation family with Robin cleft and other skeletal defects.

Authors:  H J Stalker; B A Gray; R T Zori
Journal:  Am J Med Genet       Date:  2001-11-01

2.  MRI of the brain and cervical spinal cord in rhizomelic chondrodysplasia punctata.

Authors:  A M Bams-Mengerink; C B L M Majoie; M Duran; R J A Wanders; J Van Hove; C D Scheurer; P G Barth; B T Poll-The
Journal:  Neurology       Date:  2006-03-28       Impact factor: 9.910

3.  Cervical spinal cord compression in chondrodysplasia punctata. Case illustration.

Authors:  Benson P Yang; Stefan A Mindea; Arthur J DiPatri
Journal:  J Neurosurg       Date:  2006-03       Impact factor: 5.115

4.  Cervical instability in skeletal dysplasia. Report of 6 surgically fused cases.

Authors:  O Svensson; S Aaro
Journal:  Acta Orthop Scand       Date:  1988-02

5.  Natural history of rhizomelic chondrodysplasia punctata.

Authors:  Amy L White; Peggy Modaff; Francesca Holland-Morris; Richard M Pauli
Journal:  Am J Med Genet A       Date:  2003-05-01       Impact factor: 2.802

6.  Diagnosis of atlantoaxial subluxation in Morquio's syndrome and spondyloepiphyseal dysplasia congenita.

Authors:  E Takeda; T Hashimoto; M Tayama; M Miyazaki; E Shirakawa; Y Shiino; T Saijo; M Ito; E Naito; A H Huq
Journal:  Acta Paediatr Jpn       Date:  1991-10

7.  Risk factors of myelopathy at the atlantoaxial level in spondyloepiphyseal dysplasia congenita.

Authors:  K Nakamura; K Miyoshi; N Haga; T Kurokawa
Journal:  Arch Orthop Trauma Surg       Date:  1998       Impact factor: 3.067

Review 8.  Phenotypic variability (heterogeneity) of peroxisomal disorders.

Authors:  Hanna Mandel; Stanley H Korman
Journal:  Adv Exp Med Biol       Date:  2003       Impact factor: 2.622

9.  Filamin B deficiency in mice results in skeletal malformations and impaired microvascular development.

Authors:  Xianghua Zhou; Fei Tian; Johan Sandzén; Renhai Cao; Emilie Flaberg; Laszlo Szekely; Yihai Cao; Claes Ohlsson; Martin O Bergo; Jan Borén; Levent M Akyürek
Journal:  Proc Natl Acad Sci U S A       Date:  2007-02-26       Impact factor: 11.205

Review 10.  The genetic basis of the Pierre Robin Sequence.

Authors:  Linda P Jakobsen; Mary A Knudsen; James Lespinasse; Carmen García Ayuso; Carmen Ramos; Jean-Pierre Fryns; Merete Bugge; Niels Tommerup
Journal:  Cleft Palate Craniofac J       Date:  2006-03
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  12 in total

1.  Craniovertebral junction abnormality in a case of Joubert syndrome.

Authors:  Timothy W Vogel; Brian J Dlouhy; Arnold H Menezes
Journal:  Childs Nerv Syst       Date:  2012-01-10       Impact factor: 1.475

Review 2.  Natural history and management of cervical spine disease in chondrodysplasia punctata and coumarin embryopathy.

Authors:  Timothy W Vogel; Arnold H Menezes
Journal:  Childs Nerv Syst       Date:  2012-01-25       Impact factor: 1.475

Review 3.  Novel COL2A1 mutations causing spondyloepiphyseal dysplasia congenita in three unrelated Chinese families.

Authors:  Limin Liu; QianQian Pang; Yan Jiang; Mei Li; Ou Wang; Weibo Xia
Journal:  Eur Spine J       Date:  2016-04-08       Impact factor: 3.134

4.  Congenital axis dysmorphism in a medieval skeleton : …secunda a vertendo epistropheus….

Authors:  Luciana Travan; Paola Saccheri; Francesco Toso; Enrico Crivellato
Journal:  Childs Nerv Syst       Date:  2013-05       Impact factor: 1.475

5.  Craniovertebral fusion in an infant using struts of banked adult bone.

Authors:  Giuseppe Talamonti; Giuseppe D'Aliberti; Alberto Debernardi
Journal:  Childs Nerv Syst       Date:  2015-09-23       Impact factor: 1.475

6.  Management opinions from different centers (Rio de Janeiro).

Authors:  José Francisco M Salomão; Tatiana Protzenko Cervante; Antonio Rosa Bellas
Journal:  Childs Nerv Syst       Date:  2019-05-15       Impact factor: 1.475

7.  Recurrent attacks of headache and neck pain caused by congenital aplasia of the posterior arch of atlas in an adult.

Authors:  Kaijun Wang; Xia Li; Haiyan Lou; Benyan Luo
Journal:  BMJ Case Rep       Date:  2010-11-02

8.  Occipital-Cervical Fusion and Ventral Decompression in the Surgical Management of Chiari-1 Malformation and Syringomyelia: Analysis of Data From the Park-Reeves Syringomyelia Research Consortium.

Authors:  Travis S CreveCoeur; Alexander T Yahanda; Cormac O Maher; Gabrielle W Johnson; Laurie L Ackerman; P David Adelson; Raheel Ahmed; Gregory W Albert; Phillipp R Aldana; Tord D Alden; Richard C E Anderson; Lissa Baird; David F Bauer; Karin S Bierbrauer; Douglas L Brockmeyer; Joshua J Chern; Daniel E Couture; David J Daniels; Robert C Dauser; Susan R Durham; Richard G Ellenbogen; Ramin Eskandari; Herbert E Fuchs; Timothy M George; Gerald A Grant; Patrick C Graupman; Stephanie Greene; Jeffrey P Greenfield; Naina L Gross; Daniel J Guillaume; Gabe Haller; Todd C Hankinson; Gregory G Heuer; Mark Iantosca; Bermans J Iskandar; Eric M Jackson; Andrew H Jea; James M Johnston; Robert F Keating; Michael P Kelly; Nickalus Khan; Mark D Krieger; Jeffrey R Leonard; Francesco T Mangano; Timothy B Mapstone; J Gordon McComb; Arnold H Menezes; Michael Muhlbauer; W Jerry Oakes; Greg Olavarria; Brent R O'Neill; Tae Sung Park; John Ragheb; Nathan R Selden; Manish N Shah; Chevis Shannon; Joshua S Shimony; Jodi Smith; Matthew D Smyth; Scellig S D Stone; Jennifer M Strahle; Mandeep S Tamber; James C Torner; Gerald F Tuite; Scott D Wait; John C Wellons; William E Whitehead; David D Limbrick
Journal:  Neurosurgery       Date:  2021-01-13       Impact factor: 4.654

9.  Role of dynamic computed tomography scans in patients with congenital craniovertebral junction malformations.

Authors:  Otávio Turolo da Silva; Enrico Ghizoni; Helder Tedeschi; Andrei Fernandes Joaquim
Journal:  World J Orthop       Date:  2017-03-18

10.  A novel technique to treat acquired Chiari I malformation after supratentorial shunting.

Authors:  Adriaan R E Potgieser; Eelco W Hoving
Journal:  Childs Nerv Syst       Date:  2016-06-11       Impact factor: 1.475

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