Literature DB >> 25405196

Concomitant achondroplasia and Chiari II malformation: A double-hit at the cervicomedullary junction.

Al-Wala Awad1, Kyrieckos A Aleck1, Ratan D Bhardwaj1.   

Abstract

We report the first case of a neonate with concurrent Chiari II malformation and achondroplasia. Although rare, both these conditions contribute to several deleterious anatomical changes at the cervicomedullary junction and thus predispose to acute hydrocephalus. Although our patient was initially asymptomatic, hydrocephalus ensued several weeks after birth and required cerebral spinal fluid diversion. We discuss the potential links between the two conditions, the pathophysiology, and the important clinical implications for the management of the increased risk of hydrocephalus.

Entities:  

Keywords:  Achondroplasia; Cerebral spinal fluid diversion; Cervicomedullary junction; Chiari II malformation; Hydrocephalus; Shunt failure

Year:  2014        PMID: 25405196      PMCID: PMC4233428          DOI: 10.12998/wjcc.v2.i11.711

Source DB:  PubMed          Journal:  World J Clin Cases        ISSN: 2307-8960            Impact factor:   1.337


  29 in total

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Authors:  Martina Messing-Jünger; Andreas Röhrig
Journal:  Childs Nerv Syst       Date:  2013-09-07       Impact factor: 1.475

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Journal:  Pediatr Neurosurg       Date:  1997-04       Impact factor: 1.162

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Review 7.  The molecular and genetic basis of fibroblast growth factor receptor 3 disorders: the achondroplasia family of skeletal dysplasias, Muenke craniosynostosis, and Crouzon syndrome with acanthosis nigricans.

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Journal:  Endocr Rev       Date:  2000-02       Impact factor: 19.871

Review 8.  Syndromes, disorders and maternal risk factors associated with neural tube defects (V).

Authors:  Chih-Ping Chen
Journal:  Taiwan J Obstet Gynecol       Date:  2008-09       Impact factor: 1.705

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Journal:  Clin Genet       Date:  1992-12       Impact factor: 4.438

10.  Natural history of hydrocephalus in children with spinal open neural tube defect.

Authors:  Essam A Elgamal
Journal:  Surg Neurol Int       Date:  2012-09-28
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  1 in total

1.  Chiari 1 malformation and exome sequencing in 51 trios: the emerging role of rare missense variants in chromatin-remodeling genes.

Authors:  Aldesia Provenzano; Andrea La Barbera; Mirko Scagnet; Angelica Pagliazzi; Giovanna Traficante; Marilena Pantaleo; Lucia Tiberi; Debora Vergani; Nehir Edibe Kurtas; Silvia Guarducci; Sara Bargiacchi; Giulia Forzano; Rosangela Artuso; Viviana Palazzo; Ada Kura; Flavio Giordano; Daniele di Feo; Marzia Mortilla; Claudio De Filippi; Gianluca Mattei; Livia Garavelli; Betti Giusti; Lorenzo Genitori; Orsetta Zuffardi; Sabrina Giglio
Journal:  Hum Genet       Date:  2020-12-18       Impact factor: 4.132

  1 in total

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